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
反応式
[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]参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
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%).
出典と根拠
- ORDレコード
- ord-55b4529ad25847ca98af772090262a73
- 出典データセット
- uspto-grants-2001_06
- 特許番号
- US06252086B1
反応ノート
読み込み中…