Hydrochloric Acid → (s)-(z)-5-[[5-Fluoro-2-oxo-4-[(pyrrolidin-2-yl)ethynyl]-1,2-dihydro-indol-3-ylidene]methyl]-4-methyl-1h-pyrrole-3-carboxylic acid ethyl ester hydrochloride salt
반응식
[CH2:1]([O:3][C:4]([C:6]1[C:10]([CH3:11])=[C:9](/[CH:12]=[C:13]2\[C:14](=[O:30])[NH:15][C:16]3[C:21]\2=[C:20]([C:22]#[C:23][C@@H:24]2[CH2:28][CH2:27][CH2:26][NH:25]2)[C:19]([F:29])=[CH:18][CH:17]=3)[NH:8][CH:7]=1)=[O:5])[CH3:2].[ClH:31]>O1CCOCC1>[ClH:31].[CH2:1]([O:3][C:4]([C:6]1[C:10]([CH3:11])=[C:9](/[CH:12]=[C:13]2\[C:14](=[O:30])[NH:15][C:16]3[C:21]\2=[C:20]([C:22]#[C:23][C@@H:24]2[CH2:28][CH2:27][CH2:26][NH:25]2)[C:19]([F:29])=[CH:18][CH:17]=3)[NH:8][CH:7]=1)=[O:5])[CH3:2]참가 물질
4
반응물 2
생성물 1
시약·촉매·용매 1
실험 절차
A solution of (S)-(Z)-5-[[5-Fluoro-2-oxo-4-[(pyrrolidin-2-yl)ethynyl]-1,2-dihydro-indol-3-ylidene]methyl]-4-methyl-1H-pyrrole-3-carboxylic acid ethyl ester (14 mg, 0.03 mmol) (from Example 121 above) in dioxane (10 mL) was treated with aqueous HCl under vigorous stirring. (S)-(Z)-5-[[5-Fluoro-2-oxo-4-[(pyrrolidin-2-yl)ethynyl]-1,2-dihydro-indol-3-ylidene]methyl]-4-methyl-1H-pyrrole-3-carboxylic acid ethyl ester hydrochloride salt was obtained upon lyophilization. (Yield 12 mg, 79%).
출처 및 근거
- ORD 기록
- ord-3fb7953d02e54798ad003b7405aeb0b4
- 출처 데이터셋
- uspto-grants-2001_10
- 특허 번호
- US06303793B1
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