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【结 构 式】

【分子编号】68322

【品名】N-(5-chloropyridin-2-yl)-5-methoxy-2-nitrobenzamide

【CA登记号】 

【 分 子 式 】C13H10ClN3O4

【 分 子 量 】307.69292

【元素组成】C 50.75% H 3.28% Cl 11.52% N 13.66% O 20.8%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(III)

Coupling of 5-methoxy-2-nitrobenzoic acid (I) with 2-amino-5-chloropyridine (II) by means of POCl3 and pyridine , optionally in acetonitrile solution , yields the corresponding amide (III) , which is then subjected to nitro group reduction to give amine (IV) by either treatment with SnCl2·H2O in refluxing EtOAc or catalytic hydrogenation over sulfided Pt/C in EtOAc or CH2Cl2 . Acylation of aniline (IV) with 4-cyanobenzoyl chloride (V) in the presence of pyridine in CH2Cl2 or THF affords diamide (VI). Finally, nitrile (VI) is converted to amidine by either Pinner reaction with MeOH and HCl in EtOAc and subsequent treatment of the intermediate imino ether with Me2NH in refluxing MeOH , or direct addition of lithium dimethylamide (generated from Me2NH and HexLi) to the cyano group in cold THF .
In an altenative procedure, betrixaban is obtained by coupling of aniline (IV) with the 4-amidinobenzoic acid (VII) in the presence of EDC and a catalytic amount of HCl in DMF or DMA .

1 Zhu, B.-Y., Wang, L., Goldman, E. et al. (Millennium Pharmaceuticals, Inc.). Benzamides and related inhibitors of factor Xa. EP 1259485, US 6376515, WO 200106442, WO 2001064643.
2 Zhang, P., Huang, W., Wang, L. et al. Discovery of betrixaban (PRT054021), N-(5-chloropyridin-2-yl)-2-(4-(N,N-dimethylcarbamimidoyl) benzamido)-5-methoxybenzamide, a highly potent, selective, and orally efficacious factor Xa inhibitor. Bioorg Med Chem Lett 2009, 19(8):2179-85.
3 Kanter, J.P., Sujino, K., Zuberi, S.S. (Millennium Pharmaceuticals, Inc.).WO 2008057972.
4 Pandey, A., Leitao, E.P.T., Rato, J., Song, Z.J. (Millennium Pharmaceuticals, Inc.; Merck & Co., Inc.). Methods of synthesizing factor Xa inhibitors. EP 2513058, US 201131927, WO 201108419.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 68321 5-methoxy-2-nitrobenzoic acid;2-Nitro-5-methoxybenzoic acid   C8H7NO5 详情 详情
(II) 18559 5-Chloro-2-pyridinylamine; 5-Chloro-2-pyridinamine; 2-Amino-5-chloropyridine 1072-98-6 C5H5ClN2 详情 详情
(III) 68322 N-(5-chloropyridin-2-yl)-5-methoxy-2-nitrobenzamide   C13H10ClN3O4 详情 详情
(IV) 68323 2-amino-N-(5-chloropyridin-2-yl)-5-methoxybenzamide   C13H12ClN3O2 详情 详情
(V) 19280 4-cyanobenzoyl chloride 6068-72-0 C8H4ClNO 详情 详情
(VI) 68324 N-(5-chloropyridin-2-yl)-2-(4-cyanobenzamido)-5-methoxybenzamide   C21H15ClN4O3 详情 详情
(VII) 68325 4-(N,N-dimethylcarbamimidoyl)benzoic acid hydrochloride   C10H12N2O2.HCl 详情 详情
Extended Information