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【结 构 式】

【分子编号】44036

【品名】phenyl (6S)-7-chloro-6-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-7-oxoheptanoate

【CA登记号】

【 分 子 式 】C21H18ClNO5

【 分 子 量 】399.83036

【元素组成】C 63.08% H 4.54% Cl 8.87% N 3.5% O 20.01%

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:(I)

The condensation of acyl chloride (I) with hexahydropyridazine (II) gives the corresponding amide (III), which is debenzylated with H2 over Pd/C and cyclized by means of SOCl2 to yield the pyridazinodiazepinedione (IV). Selective reduction of (IV) with borane in THF affords the pyridazinodiazepinone (V), which is treated with hydrazine to provide (1S,9S)-9-amino-10-oxoperhydropyridazino[1,2-a]azepine-1-carboxylic acid tert-butyl ester (VI). Finally, this compound is condensed with 4-phenyl-2(R)-(trifluoromethanesulfonyloxy)butyric acid ethyl ester (VII) and selectively hydrolyzed to afford the target carboxylic acid.

1 Natoff, I.L.; Redshaw, S.; Angiotensin-converting enzyme inhibitors - Cilazapril and other bicyclic hexahydropyridazines. Drugs Fut 1987, 12, 5, 475.
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) 44036 phenyl (6S)-7-chloro-6-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-7-oxoheptanoate C21H18ClNO5 详情 详情
(II) 44037 di(tert-butyl) (3S)tetrahydro-1,3(2H)-pyridazinedicarboxylate C14H26N2O4 详情 详情
(III) 44038 di(tert-butyl) (3S)-2-[(2S)-2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-6-oxo-6-phenoxyhexanoyl]tetrahydro-1,3(2H)-pyridazinedicarboxylate C34H41N3O9 详情 详情
(IV) 44039 tert-butyl (1S,9S)-9-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-6,10-dioxooctahydro-6H-pyridazino[1,2-a][1,2]diazepine-1-carboxylate C22H25N3O6 详情 详情
(V) 44040 tert-butyl (1S,9S)-9-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-10-oxooctahydro-6H-pyridazino[1,2-a][1,2]diazepine-1-carboxylate C22H27N3O5 详情 详情
(VI) 44041 tert-butyl (1S,9S)-9-amino-10-oxooctahydro-6H-pyridazino[1,2-a][1,2]diazepine-1-carboxylate C14H25N3O3 详情 详情
(VII) 20818 ethyl (2R)-4-phenyl-2-[[(trifluoromethyl)sulfonyl]oxy]butanoate C13H15F3O5S 详情 详情
Extended Information