Sodium Hydroxide → 4-(2-tert-Butoxycarbonylamino-2-cyclohexyl-acetyl)-1-cyclopropanecarbonyl-octahydro-pyrrolo[3,2-b]pyrrole-3-carboxylic acid
反応式
C[O:2][C:3]([CH:5]1[CH2:9][N:8]([C:10]([CH:12]2[CH2:14][CH2:13]2)=[O:11])[CH:7]2[CH2:15][CH2:16][N:17]([C:18](=[O:34])[CH:19]([NH:26][C:27]([O:29][C:30]([CH3:33])([CH3:32])[CH3:31])=[O:28])[CH:20]3[CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]3)[CH:6]12)=[O:4].[OH-].[Na+]>CO>[C:30]([O:29][C:27]([NH:26][CH:19]([CH:20]1[CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]1)[C:18]([N:17]1[CH:6]2[CH:7]([N:8]([C:10]([CH:12]3[CH2:13][CH2:14]3)=[O:11])[CH2:9][CH:5]2[C:3]([OH:4])=[O:2])[CH2:15][CH2:16]1)=[O:34])=[O:28])([CH3:33])([CH3:31])[CH3:32]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 44 (580 mg, 1.21 mmol) in MeOH (20 mL) was treated with 1M NaOH (4 mL) at ambient temperature. After 4 h, the solution was concentrated and diluted with EtOAc and 1M HCl. The layers were separated and the aqueous phase was extracted with EtOAc. The combined organic extracts were washed successively with 1M HCl, and brine, dried over anhydrous Na2SO4, filtered and concentrated to afford 45 (613 mg) as a yellow-colored foam which was used without further purification. Mass spectrum, m/z [464.6] (M+H)+.
後処理
- concentrationthe solution was concentrated
- additiondiluted with EtOAc and 1M HCl
- customThe layers were separated
- extractionthe aqueous phase was extracted with EtOAc
- washThe combined organic extracts were washed successively with 1M HCl, and brine
- dry with materialdried over anhydrous Na2SO4
- filtrationfiltered
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-ebfc484d18ba42c5a005b916bbe3611a
- 出典データセット
- uspto-grants-2013_07
- 特許番号
- US08481495B2
反応ノート
読み込み中…