Isopropyl Acetate → (3R,5S)-5-biphenyl-4-ylmethyl-3-methyl-2-oxo-pyrrolidine-1-carboxylic acid tert-butyl ester

HRID 588314ノート

反応式

HRID 588314 の反応式
C(OC(C)C)(=O)C.[C:8]([O:12][C:13]([N:15]1[C@H:19]([CH2:20][C:21]2[CH:26]=[CH:25][C:24]([C:27]3[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=3)=[CH:23][CH:22]=2)[CH2:18][C:17](=[CH2:33])[C:16]1=[O:34])=[O:14])([CH3:11])([CH3:10])[CH3:9].[H][H]>[Pd]>[C:8]([O:12][C:13]([N:15]1[C@H:19]([CH2:20][C:21]2[CH:22]=[CH:23][C:24]([C:27]3[CH:28]=[CH:29][CH:30]=[CH:31][CH:32]=3)=[CH:25][CH:26]=2)[CH2:18][C@@H:17]([CH3:33])[C:16]1=[O:34])=[O:14])([CH3:11])([CH3:9])[CH3:10].[C:8]([O:12][C:13]([N:15]1[C@H:19]([CH2:20][C:21]2[CH:22]=[CH:23][C:24]([C:27]3[CH:28]=[CH:29][CH:30]=[CH:31][CH:32]=3)=[CH:25][CH:26]=2)[CH2:18][C@H:17]([CH3:33])[C:16]1=[O:34])=[O:14])([CH3:11])([CH3:9])[CH3:10]

参加物

6

実験手順

Isopropyl acetate (1 ml) is added to a mixture of 100 mg (R)-5-biphenyl-4-ylmethyl-3-methylene-2-oxo-pyrrolidine-1-carboxylic acid tert-butyl ester (4-a, R1=Boc) and 10% palladium on carbon (10 mg, 50% water wet, Degussa type E101 NE/W). Hydrogen gas is applied to the mixture. The mixture is stirred at ambient temperature and pressure for 24 h. The mixture is then filtered over Celite and washed with isopropyl acetate (2×0.5 ml). The mixture is then concentrated in vacuo to give (3R,5S)-5-biphenyl-4-ylmethyl-3-methyl-2-oxo-pyrrolidine-1-carboxylic acid tert-butyl ester (3-a, R1=Boc) and (3S,5S)-5-biphenyl-4-ylmethyl-3-methyl-2-oxo-pyrrolidine-1-carboxylic acid tert-butyl ester (3-b, R1=Boc). Diastereomer ratio 15:85 (3-a, R1=Boc): 3-b, R1=Boc) as determined by hplc. Spectroscopic data in described in WO/2008/083967, for example, Examples 14 and 18.

後処理

  1. filtrationThe mixture is then filtered over Celite
  2. washwashed with isopropyl acetate (2×0.5 ml)
  3. concentrationThe mixture is then concentrated in vacuo

出典と根拠

ORDレコード
ord-af979457cb8447729b6216206511460f
出典データセット
uspto-grants-2016_01
特許番号
US09227934B2

反応ノート

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