Hydrochloric Acid → HCID 178441666、化合物
反応式
[CH2:1]([C:5]1[N:9]([CH2:10][C:11]2[CH:16]=[CH:15][C:14]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=3[C:23]3[N:27](C(OCC)C)[N:26]=[N:25][N:24]=3)=[CH:13][CH:12]=2)[C:8]([C:33]([C:35]2[CH:40]=[CH:39][CH:38]=[C:37]([CH2:41][N:42]([CH2:45][CH3:46])[CH2:43][CH3:44])[N:36]=2)=[O:34])=[C:7]([Cl:47])[N:6]=1)[CH2:2][CH2:3][CH3:4].Cl.[OH-].[Na+]>O1CCCC1>[CH2:1]([C:5]1[N:9]([CH2:10][C:11]2[CH:16]=[CH:15][C:14]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=3[C:23]3[NH:27][N:26]=[N:25][N:24]=3)=[CH:13][CH:12]=2)[C:8]([C:33]([C:35]2[CH:40]=[CH:39][CH:38]=[C:37]([CH2:41][N:42]([CH2:43][CH3:44])[CH2:45][CH3:46])[N:36]=2)=[O:34])=[C:7]([Cl:47])[N:6]=1)[CH2:2][CH2:3][CH3:4]参加物
5
実験手順
21 mg (0.032 mmole) of the compound obtained in step 1 was dissolved in 0.5 ml of tetrahydrofuran and to the resulting solution was added 0.3 ml of aqueous 1N HCl solution. The resultant was stirred for 5 hours at room temperature, neutralized with aqueous 1N NaOH solution, concentrated under reduced pressure and purified with silica gel column chromatography to obtain 16 mg of the title compound (yield 85.8%).
後処理
- concentrationconcentrated under reduced pressure
- custompurified with silica gel column chromatography
出典と根拠
- ORDレコード
- ord-e9a07be3ae3446d8a6027ff2cfde74b7
- 出典データセット
- uspto-grants-1997_09
- 特許番号
- US05665738
反応ノート
読み込み中…