(+)-Benzyl 3-{1-(1,3-benzodioxol-5-yl)-2-[(2-methoxy-4-methylphenyl)sulfonylamino]-2-oxoethyl}-1-methyl-1H-indole-6-carboxylate → (s)-(+)-3-{1-(1,3-Benzodioxol-5-yl)-2-[(2-methoxy4-methylphenyl)-sulfonylamino]-2-oxoethyl}-1-methyl-1h-indole-6-carboxylic acid
반응식
[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([CH:10]([C:26]3[C:34]4[C:29](=[CH:30][C:31]([C:35]([O:37]CC5C=CC=CC=5)=[O:36])=[CH:32][CH:33]=4)[N:28]([CH3:45])[CH:27]=3)[C:11]([NH:13][S:14]([C:17]3[CH:22]=[CH:21][C:20]([CH3:23])=[CH:19][C:18]=3[O:24][CH3:25])(=[O:16])=[O:15])=[O:12])=[CH:9][C:4]=2[O:3][CH2:2]1.[H][H]>C(O)C.[Pd]>[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([C@@H:10]([C:26]3[C:34]4[C:29](=[CH:30][C:31]([C:35]([OH:37])=[O:36])=[CH:32][CH:33]=4)[N:28]([CH3:45])[CH:27]=3)[C:11]([NH:13][S:14]([C:17]3[CH:22]=[CH:21][C:20]([CH3:23])=[CH:19][C:18]=3[O:24][CH3:25])(=[O:15])=[O:16])=[O:12])=[CH:9][C:4]=2[O:3][CH2:2]1참가 물질
5
반응물 2
생성물 1
시약·촉매·용매 2
실험 절차
(+)-Benzyl 3-{1-(1,3-benzodioxol-5-yl)-2-[(2-methoxy-4-methylphenyl)sulfonylamino]-2-oxoethyl}-1-methyl-1H-indole-6-carboxylate (from (f), 374 mg) was dissolved in aqueous ethanol (20 ml of 9:1 ethanol/water) and 50 mg of 5% palladium on carbon was added. After 3 h at 414 kPa (60 psi) of hydrogen at room temperature a further 50 mg of catalyst was added and the hydrogenation continued for a further 3 h. The catalyst was removed by filtration and the filtrate evaporated. The residue was azeotroped several times with dichloromethane to give the title compound (290 mg) in >98%ee (determined by chiral HPLC).
후처리
- customThe catalyst was removed by filtration
- customthe filtrate evaporated
- customThe residue was azeotroped several times with dichloromethane
출처 및 근거
- ORD 기록
- ord-312d3259164d4ed48f98af1cdaf6f658
- 출처 데이터셋
- uspto-grants-2001_04
- 특허 번호
- US06211223B1
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