Synthesis of pyrrolo[2,1-f][1,2,4]triazin-4(3H)-ones: Rearrangement of pyrrolo[1,2-d][1,3,4]oxadiazines and regioselective intramolecular cyclization of 1,2-biscarbamoyl-substituted 1H-pyrroles

Pyrrolo[2,1-f][1,2,4]triazin-4(3H)-ones 12 have been easily prepared via nucleophile-induced rearrangement of pyrrolooxadiazines 11 and regioselective intramolecular cyclization of 1,2-biscarbamoyl-substituted 1H-pyrroles 10. In this work, we demonstrated that the described synthetic approaches can be considered to be more facile and practical than previously reported procedures.

ple, these cyclization methods involve procedures such as microwave-assisted heating with NaOMe [1] and H 2 N-Ar [6] at 150-160 °C, refluxing with HC(OEt) 3 [3] and xylene [4,5,8], stirring at 100 °C in the presence of either NaOH or KOH [4,9], and heating with POCl 3 [11] (Figure 2). It is reasonable to consider that these harsh conditions are required because it is difficult to form the N-imine structure and to subsequently perform intramolecular cyclization ( Figure 2).
In our efforts to discover drugs that are PI3K inhibitors, a Hutchison Medipharma patent caught our attention. They reported that pyrrolotriazinones showed excellent inhibitory activities against PI3K enzymes [9]. However, their synthetic method to prepare the target molecule 9 demonstrated a limited scope, and involved high temperature, long reaction time, and low yield (approach A, Scheme 1). Another synthetic approach, reported by researchers at Infinity Pharmaceuticals Inc., has been used to obtain triazinone 12a' via rearrangement of oxadiazines 11a' (approach B, Scheme 1) [10].
However, in our investigation of the reported rearrangement reaction, the desired product 12a' was not accessed (approach B, Scheme 1). For the procedure using silica-gel column chromatography to afford triazinone 12a' from the free amine-containing oxadiazine 11a' [10], compound 11a' was not present after the boc-deprotection reaction because of its instability in the acidic conditions.
Based on the literature and the attempts reported herein, it should be highlighted that limitations exist for the preparation of the desired compounds 12. Due to these difficulties, we have investigated the synthesis of pyrrolotriazinones 12 by using a Scheme 1: Synthesis of pyrrolotriazinones 9 and 12 [9,10,18]. more convenient and facile approach than those that have been previously reported in the literature [9][10][11][12].

Results and Discussion
Our studies started with the synthesis of aminopyrrolocarbamate 10. The preparation of compound 10, which is illustrated in Scheme 2, involved chlorination of 3-chloro-1H-pyrrole-2carboxylic acid (13) using the Vilsmeier reagent [9], followed by further amination to produce 1H-pyrrole-2-carboxamide 14 in good to excellent yield [9]. A reaction mixture of 14 with NaOH, NH 4 Cl, and NaClO led to the formation of the N-aminopyrrole 15 [11]. The addition of the NH 2 + to the nitrogen of pyrrole 14 by using the NaOH/NH 4 Cl/NaClO system [11] can be considered as a more practical method than others, such as those that use NH 2 Cl and HOSA [19]. In contrast to other substituents, 2-fluorophenyl and 4-cyanophenyl groups caused low yields (15b: 15%, 15f: 31%). The N-aminopyrroles 15 were then reacted with EDC·HCl and Boc- L-alanine in THF to give the desired aminopyrrolocarbamate 10 in good to excellent yield [9].
To synthesize the desired pyrrolotriazinones 12 regioselectively we initially considered the work of Mazurkiewicz [20,21]. He reported that a mixture of 4H-3,1-benzoxazines (O-imidoylation products) and 4-quinazolones (N-imidoylation products) could be obtained after heating N-acylanthranilamides in CH 2 Cl 2 under reflux with PPh 3 Br 2 in the absence of triethylamine. In his research, it was proved that HCl or HBr influenced the rearrangement of benzoxazines to quinazolones. Importantly, triethylamine was considered to be an HBr captor [20,21].
With regard to Mazurkiewicz's work, the effect of Et 3 N on intramolecular cyclization was explored, and the acid-assisted rearrangement was also evaluated.
As shown in Table 1, although all of the obtained yields were influenced by the amount of Et 3 N, the attempt to synthesize compound 12a directly by optimizing the amount of base was not successful. For example, no reaction was observed in the absence Et 3 N (entry 1, Table 1). When excess amounts of base were used, compounds 11a and 12a were only obtained in low yields (40% combined yield, entry 3, Table 1). Alternatively, when 2.5 equivalents of Et 3 N were used, the two regioisomers 11a and 12a were obtained in an excellent overall yield of 87% (entry 2, Table 1). In addition, the ratio of 11a to 12a was not significantly affected by reaction times and temperatures (entries 4-6, Table 1).
Although initial attempts to synthesize pyrrolotriazinone 12a regioselectively were not successful, it should be highlighted that the regioisomers oxadiazine 11a and triazinone 12a could be easily prepared under very mild conditions (0 °C for 5 min), whereas only the oxadiazine 11a had been obtained in other reported procedures [10,12].
The acid-promoted rearrangement of oxadiazine 11 to triazinone 12 was also examined. However, the trial reaction was not successful because compound 11 did not tolerate acidic conditions.
Next, the effect of different halogens on the regioselectivity of the cyclization of 10 was investigated (Table 3). In general, the mixture of oxadiazines 11 and triazinones 12 was obtained in 45-98% overall yield. The results show that the regioselectivity is highly dependent on the halogen used. In particular, when PPh 3 Cl 2 was used, triazinones 12 (N-imidoylation product) were more easily obtained than oxadiazines 11 (entries 1 and 4-6, Table 3). In the case of bromine, the O-imidoylation products 11 were preferred over the N-imidoylation products 12, whereas for substrates with 2-and 3-fluorophenyl groups different results were obtained (entries 2 and 8-11, Table 3). Based on the literature results [9][10][11][12][22][23][24][25] and the reactions that are reported herein, the O-imidoylation product 11 is more accessible than the N-imidoylation product 12 when PPh 3 -Br 2 /I 2 -Et 3 N/DIPEA systems are applied (entries 2, 3, 10 and 11, Table 3).
Interestingly, in the case of the 4-cyanophenyl group, it appeared that the different reaction patterns might be a result of the reagents PPh 3 Br 2 and PPh 3 Cl 2 (entries 7 and 12, Table 3). For alkyl substituents (4-methoxybenzyl and cyclopropyl, entries 13 and 14, Table 3), triazinones 12g and 12h were selectively prepared in over 60% yield. Based on these results, it is possible to consider that due to the presence of electron-donating groups, such as alkyl substituents, only the N-imidoylation products 12g, and 12h were formed.
It is possible to propose a reaction mechanism after considering our studies and the literature results ( Figure 3) [20][21][22][23][24][25][26][27][28]. For example, it is not reasonable to consider Mazurkiewicz's acid-promoted rearrangement [20,21], because oxadiazine is not stable under acidic conditions. In the case of the rearrangement of 11a to 12a, the mechanism of the nucleophile-induced cyclization is proposed after considering Hart's research on the synthesis of fumiquinazolines [22]. It was shown that the nucleophilicity of the N-acylnitrenium ion was increased when the oxygen ion was stabilized by counter ions such as lithium and sodium. For the intramolecular cyclization step, it was shown that the regioselectivity depends on the halogen source (Br/Cl) and neighboring groups of the N-acylnitrenium ions (electronwithdrawing aryl and -donating alkyl substitutents). This is highlighted by the observation that the N-imidoylation product (triazinone) 12 was preferentially obtained when a chlorinehalogen source and electron-donating alkyl groups were used. While further studies are required, we suggest the intermediates are N-acylnitrenium ions [26] and halogen-imine structures (the Vilsmeier type) [27,28].
Because oxadiazines 11 and triazinones 12 are non-crystalline, their exact structures were assigned by NMR spectroscopy ( 1 H and 13 C). With the literature results alone [9][10][11][12] the identity of the regioisomers could not be accurately confirmed; therefore, the NMR studies were required. As shown in Table 4, different NOEs were observed for compounds 11 and 12.
Upon examination of the 1 H NMR spectra of oxadiazines 11 and triazinones 12, different peak patterns of the NH protons  were observed (11 -NH: 4.8 ppm, 12 -NH: 5.1 ppm, see Supporting Information File 1).
Through 13 C NMR and IR analysis the presence of two regioisomers could be confirmed by the peaks of specific functional groups ( Figure 4).
According to the NMR and IR data, compounds 11 and 12 are believed to have pyrrolooxadiazine and pyrrolotriazinone structures, respectively. Notably, this is the first report in which the exact structures of these regioisomers have been determined.
Notably, we found that triazinones 12 can be readily accessed under very mild conditions (0 °C, 5 min). The regioselectivity was influenced by the identities of halogen sources of triphenylphosphorane and the N-functional groups. For the rearrangement reaction, it was demonstrated that triazinone 12a was easily obtained when counter ions of oxygen such as lithium and sodium were used. Finally, we predict that these methods could be useful for the preparation of biologically active pyrrolotriazinones and -triazines.