【结 构 式】 |
【分子编号】43959 【品名】N-isopropylbenzenecarboximidoyl chloride 【CA登记号】 |
【 分 子 式 】C10H12ClN 【 分 子 量 】181.66472 【元素组成】C 66.12% H 6.66% Cl 19.52% N 7.71% |
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:(XV)Resolution of (XII) by chiral HPLC and then acetylation of the hydroxyl group gave the chiral acetate (XIII). The pyridine ring of (XIII) was converted to the corresponding N-oxide (XIV) by means of meta-chloroperbenzoic acid. Subsequent displacement of the N-oxide of (XIV) with N-isopropyl-benzimidoyl chloride (XV) introduced the N-benzoyl-N-isopropylamino group into the pyridine to afford (XVI). After tert-butyl ester cleavage with trifluoroacetic acid, yielding (XVIII), basic hydrolysis of the benzamido group provided the title compound.
【1】 Hayama, T.; Ohtake, N.; Niiyama, K.; et al.; New cyclopentenopyridine derivatives. A potent, orally active, selective endothelin ETA receptor antagonist. 16th Int Symp Med Chem (Sept 18 2000, Bologna) 2000, Abst PA-78. |
【2】 Nishikibe, M.; Hayama, T.; Otake, N. (Banyu Pharmaceutical Co., Ltd.); Substd. 5-(2,2-difluoro-1,3-benzodioxol-5-yl) cyclopentenopyridine deriv.. EP 1049691; WO 9937639 . |
中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
---|---|---|---|---|---|---|
(XII) | 43955 | tert-butyl (5S,6R,7R)-5-(2,2-difluoro-1,3-benzodioxol-5-yl)-7-[2-(3-hydroxy-2-methylpropyl)-4-methoxyphenyl]-6,7-dihydro-5H-cyclopenta[b]pyridine-6-carboxylate | C31H33F2NO6 | 详情 | 详情 | |
(XIII) | 43957 | tert-butyl (5S,6R,7R)-7-[2-[3-(acetoxy)-2-methylpropyl]-4-methoxyphenyl]-5-(2,2-difluoro-1,3-benzodioxol-5-yl)-6,7-dihydro-5H-cyclopenta[b]pyridine-6-carboxylate | C33H35F2NO7 | 详情 | 详情 | |
(XIV) | 43958 | (5S,6R,7R)-7-[2-[3-(acetoxy)-2-methylpropyl]-4-methoxyphenyl]-6-(tert-butoxycarbonyl)-5-(2,2-difluoro-1,3-benzodioxol-5-yl)-6,7-dihydro-5H-cyclopenta[b]pyridinium-1-olate | C33H35F2NO8 | 详情 | 详情 | |
(XV) | 43959 | N-isopropylbenzenecarboximidoyl chloride | C10H12ClN | 详情 | 详情 | |
(XVI) | 43960 | tert-butyl (5S,6R,7R)-2-[benzoyl(isopropyl)amino]-5-(2,2-difluoro-1,3-benzodioxol-5-yl)-7-[2-(3-hydroxy-2-methylpropyl)-4-methoxyphenyl]-6,7-dihydro-5H-cyclopenta[b]pyridine-6-carboxylate | C41H44F2N2O7 | 详情 | 详情 | |
(XVII) | 43961 | (5S,6R,7R)-2-[benzoyl(isopropyl)amino]-5-(2,2-difluoro-1,3-benzodioxol-5-yl)-7-[2-(3-hydroxy-2-methylpropyl)-4-methoxyphenyl]-6,7-dihydro-5H-cyclopenta[b]pyridine-6-carboxylic acid | C37H36F2N2O7 | 详情 | 详情 |
Extended Information