Hydrochloric Acid → HCID 86646923、化合物

HRID 221497

反応式

[CH2:1]([O:3][C:4]([O:6][CH2:7][CH2:8][O:9][C:10]([C:12]1[N:13]=[C:14]([C:43]([F:46])([F:45])[F:44])[N:15]2[CH2:20][CH2:19][N:18]([C:21](=[O:42])[CH2:22][C@H:23]([NH:34]C(OC(C)(C)C)=O)[CH2:24][C:25]3[CH:30]=[C:29]([F:31])[C:28]([F:32])=[CH:27][C:26]=3[F:33])[CH2:17][C:16]=12)=[O:11])=[O:5])[CH3:2].[ClH:47]>C(OCC)(=O)C>[ClH:47].[CH2:1]([O:3][C:4]([O:6][CH2:7][CH2:8][O:9][C:10]([C:12]1[N:13]=[C:14]([C:43]([F:44])([F:45])[F:46])[N:15]2[CH2:20][CH2:19][N:18]([C:21](=[O:42])[CH2:22][C@H:23]([NH2:34])[CH2:24][C:25]3[CH:30]=[C:29]([F:31])[C:28]([F:32])=[CH:27][C:26]=3[F:33])[CH2:17][C:16]=12)=[O:11])=[O:5])[CH3:2]

参加物

実験手順

(R)-7-[3-tert-Butoxycarbonylamino-4-(2,4,5-trifluoro-phenyl)-butyryl]-3-trifluoromethyl-5,6,7,8-tetrahydro-imidazo[1,5-a]pyrazine-1-carboxylic acid (1-ethoxycarbonyloxy)-ethyl ester 34a (0.26 g, 0.39 mmol) and 5 mL of ethyl acetate were added into the reaction flask. A solution of 6.5 N hydrochloric acid in 3 mL of ethyl acetate was then added to the flask. The reaction mixture was stirred at room temperature for 6 hours and monitored by thin layer chromatography until the disappearance of the starting materials. The reaction mixture was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain the title compound (R)-7-[3-amino-4-(2,4,5-trifluoro-phenyl)-butyryl]-3-trifluoromethyl-5,6,7,8-tetrahydro-imidazo[1,5-a]pyrazine-1-carboxylic acid (1-ethoxycarbonyloxy)-ethyl ester hydrochloride 34 (0.2 g, yield 85%) as a white solid.

後処理

concentrationThe reaction mixture was concentrated under reduced pressure
customThe resulting residue was purified by silica gel column chromatography

出典と根拠

ORDレコード: ord-52815ee926814c2a8b62cbd6469365da
出典データセット: uspto-grants-2012_06
DOI: 10.6084/m9.figshare.5104873.v1
特許番号: US08207161B2

反応式

参加物

反応物 2

生成物 1

試薬・触媒・溶媒 1

実験手順

後処理

出典と根拠

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