Synthesis of (Z)-3-[amino(phenyl)methylidene]-1,3-dihydro-2H-indol-2-ones using an Eschenmoser coupling reaction

A highly modular method for the synthesis of (Z)-3-[amino(phenyl/methyl)methylidene]-1,3-dihydro-2H-indol-2-ones starting from easily available 3-bromooxindoles or (2-oxoindolin-3-yl)triflate and thioacetamides or thiobenzamides is described. A series of 49 compounds, several of which have previously been shown to possess significant tyrosin kinase inhibiting activity, was prepared in yields varying mostly from 70 to 97% and always surpassing those obtained by other published methods. The method includes an Eschenmoser coupling reaction, which is very feasible (even without using a thiophile except tertiary amides) and scalable. The (Z)-configuration of all products was confirmed by NMR techniques.


Introduction
3-(Aminomethylidene)-1,3-dihydro-2H-indol-2-ones (3-(aminomethylidene)oxindoles) belong to a subclass of intensively studied heterocyclic compounds, especially due to their significant pharmacological activity. As early as in the middle of the 1980s researchers at Pfizer Inc. patented [1] these compounds as highly potent gabaergic agents, having possible therapeutic utility as anticonvulsants or anxiolytics [2]. However, the main therapeutic potential of these compounds was discovered ca 15 years later when several patents appeared claiming their inhibiting effect on various kinases [3,4]. Since that time many patents as well as papers have been published [5][6][7][8][9][10][11] on that topic but until present only Nintedanib (Figure 1) was approved [12,13] for the treatment of idiopathic pulmonary fibrosis in 2014.
In our group we recently discovered [32,33] a new synthetic pathway involving a rearrangement of 2-aryl-5-(2-aminophenyl)-4-hydroxy-1,3-thiazoles (e.g., 8aa-ad in Scheme 2) leading to the 3-[amino(aryl)methylidene]-1,3-dihydro-2Hindol-2-ones containing an unsubstituted amino group and the oxindole nucleus. In the present paper, we want to describe an optimized procedure avoiding the intermediary thiazoles and to demonstrate the usefulness and wide group tolerability of our new synthetic approach for the preparation of a library of substituted phenyl and amino derivatives ( Table 1). A number of the compounds that have been prepared using this route (namely 5ac', 5ca, 5cc', 5da, 5db, and 5dc') have significant tyrosin kinase inhibiting properties [11].

Scheme 2:
The possible intermediates and products occurring in the reactions of 3-bromooxindoles with thiobenzamides.
2-aryl-5-(2-aminophenyl)-4-hydroxy-1,3-thiazoles (when starting from 2c,d) or leads to a complex and inseparable mixture of products (when starting from 2a,b). The addition of a base (e.g., triethylamine, N-methylmorpholine, ammonia) which was originally found to be beneficial [33] for the rearrangement of the kinetically formed thiazole to the desired product now caused a complete decomposition giving mainly the isoindigo derivatives 9a-e. Similar issues were observed when the secondary or tertiary thiobenzamides 3a-i or 4a-c were used. The following Scheme 2 summarizes the main possible reaction routes starting from 3-bromooxindoles 1a-e and various primary, secondary, and tertiary thiobenzamides 2a-d, 3a-i, and 4a-c.
The formation of the different products can be explained as follows. In acetonitrile, that was used in our previous study [33], the C 3 hydrogen of the initially formed α-thioiminium salt is not acidic enough to form the carbanion that is necessary for the desired Eschenmoser coupling reaction (route b). Therefore, the nucleophilicity of the conjugated base of the nitrogen (benzenecarbimidothioate or thioimidate) is exerted towards the oxindole carbonyl to give the thiazole. Moreover, if both benzene rings contain electron-withdrawing groups, enhancing either the leaving ability of the oxindole nitrogen (R 1 : Cl, NO 2 ) or the acidity of the >C=NH 2 + group (R 2 : Cl, CF 3 ) increasing the proportion of the nucleophile >C=NH, then the formation of the thiazole (route a) is further accelerated (Scheme 2). Although the addition of a base generates the required C 3 carbanion, such a base also converts the reactive α-thioiminium group to a much less reactive thioimidate at the same time. The C 3 carbanion then preferentially attacks (route c) another molecule of the starting material 1a-e and the resulting adducts undergo a subsequent elimination to give the isoindigo derivatives 9a-e. The substituent R 4 strongly influences both the equilibrium between >C=N + HR 4 and >C=NR 4 as well as the nucleophilic attack of the internal C 3 carbanion to give the thiirane intermediate in Scheme 2. While the EWG groups decrease the concentration of the α-thioiminium salt (that is much more prone to a nucleophilic addition than the free thioimidate group) they also make the α-thioiminium/thioimidate group more reactive. These two effects are antagonistic and therefore a thorough study of the R 4 substituent influence is necessary. On the other hand, mono-as well as disubstitution of the thioamide nitrogen completely prevents the formation of the thiazole (route a).
The rather complicated product isolation procedure of the Eschenmoser coupling reaction (route b) and the long reaction time taken together with problems connected with changing substituents throughout the molecule, encouraged us to find better or even universal reaction conditions compatible with all substituents present in both benzene rings (R 1 and R 2 ) as well as at the thioamide nitrogen (R 3 and R 4 ).
In order to achieve the desired product of the Eschenmoser coupling reaction (route b), two main prerequisites must be fulfilled -i.e., the substantial acidity of a hydrogen at C 3 and a more stable α-thioiminium group necessary for the internal nucleophilic addition giving the thiirane intermediate (route b). It is well known that the acidity of carbon acids in acetonitrile is much lower than in polar aprotic solvents, like DMSO or DMF or in polar protic solvents like alcohols. For carbon acids the ΔpK a is 12.9 between ACN and DMSO but the ΔpK a is only −1.5 between DMF and DMSO [34]. A change of the solvent from acetonitrile to DMF should therefore decrease the pK a by ca. 11 units. In polar protic solvents (e.g., in methanol) such an increase of acidity should be also distinct but it is known that polar protic solvents much better solvate anions and thus decrease their nucleophilicity. Therefore, dimethylformamide has been chosen as the best solvent.
Indeed, when dimethylformamide (DMF) was used as the solvent for the reaction of the substituted 3-bromooxindoles 1a-e with various aromatic primary (2a-d) and secondary (3a-i) thiobenzamides, the corresponding 3-[amino(phenyl)methylidene]oxindoles (series 5 and 6) were obtained in good yields mostly exceeding 70% without the occurrence of intermediary thiazoles (route a). Only with a few secondary thiobenzamides (3c-e) or the tertiary thiobenzamides 4b,c, the yields were lower.
Reaction of 1a-e with primary thiobenzamides 2a-d (R 3 , R 4 : H) All possible combinations of the 3-bromooxindoles 1a-e with the primary thiobenzamides 2a-d were studied in order to test the R 1 and R 2 substituent tolerance. Moreover, in order to demonstrate the application potential of our method, a few more derivatives containing R 2 : I instead of Cl (5ac', 5cc', 5dc') which display a significant kinase inhibition activity, have been prepared. It is worth noting that the existing literature synthetic pathway [11] gave only poor yields of these desirable compounds. From the data presented in Table 2, it is clear that the yields obtained in DMF are mostly very good and always much better than the previously reported yields by us in ACN [33] (see Table 2, entries 1-4) or by other authors starting from iminoesters [11] (see Table 2, entries 9, 13, 14, and 21-23). However, the inspection of Table 2 does not show any clear dependence between the electronic properties of the substituent R 1 or R 2 and the isolated yield. In most cases the yields are higher than 80%, but it seems that the presence of at least one EWG often gives an enhanced yield above 90% (cf. entries 3,4,8,9,11,15,20, and 21 in Table 2). The influence of a single substit-  [33]); b prepared from 2-(phenylethynyl)phenylisocyanate (see reference [22]); c prepared from oxindole and the corresponding benzonitrile (see reference [14]); d prepared from oxindole and benzoic acid imidoester (see reference [11]). uent R 1 is weaker (e.g., entries 1, 5, 13, and 17 in Table 2) because the electron-withdrawing groups enhance the C 3 -H acidity and an EDG enhances the C 3 carbanion nucleophilicity and these two effects are opposing. The influence of the substituent effects, as quantified using Hammett's substituent constants [35], on the yields can be represented graphically ( Figure 2).

Reaction of 1a-e with secondary thiobenzamides 3a-i
Secondary thiobenzamides 3a-i also react well with 3-bromooxindoles 1a-e (Table 3) although the average yields of the corresponding products 6aa-ef are always 10-15% lower when comparing substrates with the same R 1 (R 2 and R 3 are always H). For example, while for the reaction of 1a with 2a the yield is 88% ( Table 2, entry 1), a nitrogen substitution (3a: R 4 : C 6 H 5 or 3f: R 4 : CH 3 ) lowers the isolated yields to 77% and 76% (Table 3, entries 1 and 6), respectively. The further substitution of the N-phenyl group with an EWG causes a significant decrease in the isolated yield (cf. entries 1, and 3-5 in Table 3) from 77% to only 32% while an EDG substituent (4-OCH 3 ; entry 2 in Table 3) enhances the yield to 88%. From these observations it is clear that the influence of R 4 is much stronger than the influence of the substituent R 1 (cf. entries 1 and 10-13 or entries 6 and 14-17 in Table 3). The attached EWG substituent R 4 lowers the pK a (and thus also the equilibrium concentra-   [23]); b the E-isomer prepared from 3-bromo-3-(bromo(phenyl)methyl)-5-chlorooxindole (see reference [27]). tion) of the intermediary α-thioiminium salt which is much more reactive towards an internal nucleophilic attack than the free thioimidate group. Although an electron-withdrawing substituent R 4 also enhances the internal nucleophilic attack to both α-thioiminium and imine groups -such influence is weaker because this addition occurs on a carbon atom more distant from R 4 . The presumption that the presence of an α-thioiminium group is a necessary prerequisite for the successful reaction progress is further supported by the fact that all N-alkyl-substituted thiobenzamides 3f-i (see entries 6-9 in Table 3) give comparable yields around 70%.
Reaction of 1a-c with tertiary thiobenzamides 4a-c The preliminary experiments involving the reaction of 1a with N,N-dimethylthiobenzamide (4a) in DMF have shown that the reaction is much slower (>24 h) and also gives relatively high amounts of the undesirable isoindigo 9a [32] (route c). In order to accelerate the Eschenmoser coupling reaction and to enhance the reaction yield (route b) an addition of a suitable thiophile assisting the sulfur extrusion should be beneficial [36]. Therefore, we tested two P(III) compounds as thiophiles. First, we added triphenylphosphine (1 equiv) but an even more complex mixture of products resulted. Much better results were obtained when trimethyl phosphite was used but this strongly depended on the used molar ratio: the best yield of the product 7aa (83%) was achieved when using 1.5 equiv of trimethyl phosphite. While a lower amount (1 equiv) had only a moderate influence on the reaction progress (yield of 7aa was 50%) a higher amount (3 equiv) caused a significant reduction of 1a to the parent oxindole (yield of 7aa was 44%). Therefore, the optimized amount (1.5 equiv) was used for the synthesis starting from the other thiobenzamides 4b and 4c and 3-bromooxindoles 1b and 1c (Table 4). From the inspection of Table 4 it is obvious that the isolated yields are lower (19-60%) but this is mainly due to the requirement for a more complex separation involving repeated column chromatography and/or crystallization.

Aliphatic thioamides
Although our concern was mainly dedicated to the synthesis of 3-[amino(aryl)methylidene]oxindoles many of which display a significant tyrosin kinase inhibiting activity, we also verified the versatility of our method for the analogous oxindoles 10a-c carrying a methyl group on the methylidene carbon (Scheme 3).
The replacement of thiobenzamide and its N-methyl or N-phenyl derivative with the analogous aliphatic thioacetamides has virtually no influence on the reaction progress and the corresponding oxindoles 10a-c were obtained in 62-89% yields ( Table 5).  [14]).

Alternative electrophilic components for the Eschenmoser coupling reaction
The Eschenmoser coupling reaction [36,37] usually starts from α-substituted ketones, esters, malonates, or nitriles. The group in the α-position must be a good leaving group enabling a facile nucleophilic substitution giving the α-thioiminium salt and the cleaved leaving group should be a poor nucleophile in order to suppress the reverse reaction. In most cases halogens (mainly Br and I) fulfill these criteria but for highly congested thioamides only triflates gave desirable yields [36]. Moreover, several new alternatives to the Eschenmoser coupling reaction can be found in the recent literature [38][39][40].
In our case, the 3-bromooxindoles 1a-e worked very well but they are accessible from commercially available isatins only through a three-step synthesis in an acceptable overall yield 51-76% (see Table 6 in the Experimental). In order to avoid the relatively long synthesis of the precursors we tried to change Br for another leaving group Y (Scheme 4).
First, we prepared 3-chlorooxindole (1f) which is available from β-nitrostyrene and acetyl chloride under FeCl 3 catalysis [41]. Unfortunately, the Eschenmoser coupling reaction with thiobenzamide (2a) did not proceed at all and only the formation of isoindigo 9a was observed. However, a very easy synthesis of diethyl (2-oxoindolin-3-yl)phosphate (1g) from isatin has recently appeared [42] which encouraged us to submit this reagent to the Eschenmoser reaction. Unfortunately, this reagent reacts with the parent thiobenzamide (2a) very slowly even after heating to 80 °C. A maximum (chromatographic) yield 38% of 5aa was achieved after 32 h when a double molar excess of phosphate 1g was used. A further increase in the excess of 1g had no positive effect on the yield of 5aa. This result is in accordance with the relatively low nucleofugality of diethyl phosphate which is roughly quantified by the pK a = 1.39 of its conjugated acid [43]. We have also examined an addition of 20% of tetrabutylammonium bromide as a nucleophilic catalyst which could transform the phosphate 1g in situ to the more reactive bromo derivative 1a. It was found that such addition has only a small positive effect on the reaction progress, most probably due to only a slightly higher nucleophilicity of the bromide (n = 3.9) [44] in comparison with the thiobenzamide (n = 3.1) [45].
The last possibility for the activation of the oxindole component involves the introduction of the triflate group into position 3. The synthesis of triflates according to the standard protocol involves the reaction of an alcohol with triflic chloride or anhydride. However, these very reactive reagents could react with 3-hydroxyoxindole both on the oxygen as well as on the nitrogen. Therefore, we first examined a protocol starting from N-methylisatin which was reduced to 3-hydroxy-N-methyloxindole [46] (yield 75%; note: the reduction of other isatins gives lower yields) and then treated with triflic anhydride under inert atmosphere at −20 °C. Quite a clean formation of the triflate 1i was observed in an NMR tube but all attempts to isolate the pure compound 1i in a preparative scale failed. Therefore, we decided to carry out an Eschenmoser coupling reaction in a onepot manner. Into a chilled solution of 3-hydroxy-N-methyloxindole in DMF, one equivalent of triflic anhydride was added first and, after reaction completion, one equivalent of thiobenzamide (2a) was added. By this route, the desired product of the Eschenmoser coupling 11 was isolated in a very good yield of 87% (cf. with 78% in reference [33] and 64% in reference [14]). As a result, a good overall yield of 65% was achieved over three steps starting from N-methylisatin. For comparison, the four-step synthesis starting from N-methylisatin and giving 11 through 3-bromo-N-methyloxindole (1a'), has an overall yield of only 48%. Moreover, no formation of the isoindigo derivative was observed under such conditions -probably due to the presence of triflic acid evolved during the first step. This new route is therefore suitable for the synthesis of N-alkyl-3-(aminomethylidene)oxindoles.
We also tried to apply the same protocol for the parent (i.e. N-unprotected) 3-hydroxyoxindole and thiobenzamide (2a). We partly succeeded because we isolated the coupling product 5aa in 65% yield (48% from isatin) which is still less than when starting from isatin through 1a (57%). For a further two representatives, namely 4'-trifluoromethylthiobenzanilide (3d) and N,N-dimethylthiobenzamide (4a) the same one-pot method gives only 18% of the product 6ad (cf. with 43% from 1a) and 27% (without thiophile) of 7aa (cf. with 86% from 1a). It was obvious that an improved synthetic approach would necessitate the protection of the oxindole nitrogen avoiding the formation of the undesired N-Tf derivative. Such nitrogen protection/ deprotection (e.g., acetylation/deacetylation) is often used in the other synthetic strategies described in Scheme 1. Therefore, the starting isatin was acetylated first with acetic anhydride [47] in 95% yield and then reduced with various complex borohy-drides (e.g., sodium borohydride, sodium cyanoborohydride, or sodium triacetoxyborohydride) in methanol. Unfortunately, formation of the desired N-acetyl-3-hydroxyoxindole was not observed at all, because a base-catalyzed addition of methanol to the C 3 =O and subsequent intramolecular rearrangement of the acetyl group occurs to give 3-methoxy-2-oxoindolin-3-yl acetate. Other reducing agents recommended in the literature for the reduction of unprotected isatin (sodium dithionite, zinc, phosphinic acid, etc.) also failed or caused an acetyl group removal. Therefore, we abandoned this strategy.

Configuration of products 5-7
All 3-(aminomethylidene)oxindoles can formally exist as (Z)or (E)-isomers. Their actual configuration depends on the substitution at the methylidene carbon as well as the nitrogen. While derivatives containing an unsubstituted methylidene carbon and tertiary nitrogen exist as a mixture of rapidly equilibrating (Z)/(E)-isomers [2], the derivatives containing a secondary nitrogen slightly prefer [2,9,48] the (Z)-configuration due to an intramolecular hydrogen bond. A substitution of hydrogen at the methylidene carbon by an aryl group and a secondary nitrogen, enabling an intramolecular hydrogen bond, results in the geometry of a double bond that is locked in a (Z)-configuration [12]. The same (Z)-configuration was observed by us for the primary 3-[amino(aryl)methylidene]oxindoles [33].
The usual method used for the configuration assignment of 3-amino(aryl)methylidene derivatives involves a simple 1 H NMR experiment showing either an upfield (δ ≈ 5.7-6.4 ppm for (Z)-configuration [5,12,32,33]) or a downfield shift (δ ≈ 7.7-7.9 ppm for (E)-configuration [27]) of the proton in position 4 of the oxindole moiety. In our previous paper [32] such an assignment was also confirmed in the solid state by X-ray diffraction. The important role of the intramolecular hydrogen bond fixing the (Z)-configuration has also been observed in the crystal structures of other 3-aminomethylidene derivatives containing a primary or secondary nitrogen [14,[49][50][51][52].
The (Z)-configuration of the newly prepared 3-[amino(aryl)methylidene]oxindoles with primary, secondary, and tertiary nitrogen (series 5-7) has been therefore confirmed by 1 H NMR spectroscopy in CDCl 3 or DMSO-d 6 solution. In all spectra the proton in position 4 of the oxindole moiety shows a typical upfield shift in the range of 5.7-6.4 (series 5), 5.3-5.9 (series 6), and 5.0-5.5 ppm (series 7), except for the nitro derivatives (R 1 : 5-NO 2 ) where the nitro group always enhances the Ar-H 4 chemical shift by about 0.7 ppm. Therefore, a 2D-NOESY experiment was performed for some representative 5-NO 2 derivatives (5eb-ed) confirming their (Z)-configuration (see Supporting Information File 1).

Conclusion
We have developed an efficient and versatile synthesis of (Z)-3-[amino(phenyl/methyl)methylidene]-1,3-dihydro-2H-indol-2ones (series 5, 6, 7, 10, and compound 11) starting from 3-bromooxindoles 1a-e and primary, secondary or tertiary thioacetamides and thiobenzamides 2-4. The superiority of our method in terms of the isolated yield (mostly >70% but often >85%) is clearly seen in all relevant cases (see Table 2 and Table 3) in which a direct comparison with other preparative routes [11,14,22,23] is possible. Although the starting 3-bromooxindoles 1a-e are available from the corresponding isatins by a three-step synthesis (overall yield 51-76%), the total yields related to these commercially available and cheap starting compounds are better or at least competitive to the methods described in Scheme 1 of which several have serious disadvantages. For example, the method starting from N-phenylpropiolamides [24] is not applicable (i.e., 0% yield) for the preparation of 1-unsubstituted 3-(aminomethylidene)oxindoles and the method involving the transformation of 3-bromo-3-[bromo(phenyl)methyl]oxindoles [27] gives the products with inversed configuration of the double bond. Several synthetic strategies starting from isocyanate [22,23] or oxindole [4,12] precursors work well only with protected nitrogen(s) in the starting compounds whose preparation and protection/deprotection also lengthens the total synthesis and decreases the overall isolated yield of the desired 3-(aminomethylidene)oxindoles.
The main advantages of our synthetic approach using an Eschenmoser coupling reaction involve the easy elaboration with no need for an inert atmosphere, extra dry solvents or toxic starting compounds (e.g., triphosgene needed for the synthesis of isocyanates) and (except for tertiary thioamides) addition of a thiophile. Moreover, our method has almost no limitation in terms of substitutions on each part of the skeleton.
Our alternative and shorter synthetic approach also starts from isatin and involves its reduction to 3-hydroxyoxindole and a one-pot triflation/Eschenmoser coupling with thiobenzamides under an inert atmosphere. However, this procedure is only suited for the preparation starting from N-methyl-3-hydroxyoxindole in which excessive N-triflication is blocked and the overall yield of 1-methyl-3-(aminomethylidene)-1,3-dihydro-2H-indol-2-one (11) (to isatin) is better than those obtained through 3-bromo-N-methyloxindole (1a'). In the case of parent isatin such a strategy also gives the desired products 5aa, 6ad, and 7aa but in a lower overall yield than the yield obtained through 1a. Other leaving groups in position 3 of the oxindole are unsuitable because only very slow (phosphate) or even no Eschenmoser coupling reaction (chloride) occurs with them.

Experimental
The starting 3-bromooxindoles 1a-e and 3-bromo-N-methyloxindole (1a') were synthesized from the corresponding isatins using the procedure described in our previous paper [33] (see also Supporting Information File 1). The following Table 6 summarizes the overall yields after three steps. 3-Hydroxyoxindole and 3-hydroxy-N-methyloxindole were prepared [46] from the corresponding isatins through the reduction with sodium borohydride in methanol (see also Supporting Information File 1). The primary thiobenzamides 2a-d were prepared by the magnesium chloride-catalyzed thiolysis of commercially available benzonitriles [53] and the secondary thiobenzamides 3a-h were obtained by the thionation of the corresponding N-substituted amides [54] using pyridine-P 4 S 10 as sulfurization agent. The tertiary thiobenzamides 4a-c were synthetized by a one-pot acylation/thionation from the corresponding acid chlorides and dimethylamine [55]. Other chemicals and solvents were purchased from Acros Organics, Sigma-Aldrich, or Fluorochem and were used as received. The melting points are uncorrected. 1  General procedure for the synthesis of 3-[amino(phenyl)methylidene]-1,3-dihydro-2H-indol-2-ones (5aa-ed and 6aa-ef) In a 20 mL flask with a magnetic stirrer the solutions of the corresponding 3-bromooxindole 1a-e and substituted thiobenzamide 2a-d or 3a-i (amounts specified in Table 2 and Table 3) in dry DMF (5 + 5 mL for 3 mmol scale) were mixed and the mixture stirred for 5 h (primary thiobenzamides) or 12 h (secondary thiobenzamides) at room temperature. Then, TEA (2 equiv) was added and the mixture stirred for additional 5 min and diluted with water (100 mL). The aqueous solution was extracted with DCM (3 × 60 mL) and the combined organic layers were washed with water (2 × 40 mL) and brine (40 mL), dried with anhydrous Na 2 SO 4 and evaporated. The solid residue was dissolved in methanol and filtered through a plug of Celite.
The filtrate was evaporated with silica gel and submitted to preparative flash chromatography (silica gel or alumina cartridge; mobile phase and gradient are specified in Supporting Information File 1). Analytically pure samples were obtained by crystallization from the appropriate solvent.
Compounds 5ea and 5eb were isolated as follows: After the reaction of 1e with 2a,b (4 h) the reaction mixture was poured into cold EtOAc/EtOH 20:1 (80 mL) and stirred for 30 min. The precipitated product was filtered off and washed with EtOAc (2 × 5 mL). The crude 5ea or 5eb was dissolved in boiling CHCl 3 /CH 3 OH 1:1 (ca 125 mL) and filtered through a short plug of silica gel which was then washed with another portion (50 mL) of CHCl 3 /CH 3 OH 1:1. The collected filtrates were dried and evaporated.

Synthesis of 3-[dimethylamino(phenyl)methylidene]-1,3dihydro-2H-indol-2-ones (7aa-ca)
The 4-substituted N,N-dimethylthiobenzamide (4a-c, n 4a-c ) and trimethyl phosphite (1.5 equiv) were dissolved in a minimum amount of dry DMF and a saturated solution of 3-bromooxindole (1a-c, n 1a-c ) in dry DMF was added. The reaction mixture was stirred for 20 h at room temperature (TLC monitoring; silica gel plates/EtOAc/hexane) and then diluted with an aqueous NaHCO 3 solution (5%, 50 mL). The suspension was extracted with EtOAc (3 × 150 mL) and the combined organic layer was washed with water (5 × 100 mL), brine (2 × 100 mL), dried with anhydrous Na 2 SO 4 and evaporated. The residue was repeatedly evaporated with EtOH to remove trimethyl thiophosphate. The crude product was then submitted to preparative flash chromatography (silica gel or alumina cartridge; mobile phase and gradient are specified in the Supporting Information File 1).
Synthesis of 3-[amino(methyl)methylidene]-1,3-dihydro-2H-indol-2-ones (10a-c) The corresponding thioacetamide (2 mmol) was dissolved in DMF (5 mL) and a solution of 1a (424 mg, 2 mmol) in dry DMF (5 mL) was added. The mixture was stirred overnight at room temperature and then evaporated in vacuum. The residue was dissolved in DCM (40 mL), evaporated with neutral alumina (5 g) and submitted to preparative flash chromatography (silica gel or alumina cartridge; mobile phase and gradient are specified in Supporting Information File 1).

Supporting Information
Supporting Information File 1 Synthetic procedures, characterization data and copies of spectra.