(R)-3-(4-Benzyloxy-2,6-dichloro-benzyl)-1-(4,5,6,7-tetrahydro-1H-indazol-4-yl)-pyrrolidin-2-one → (R)-3-(2,6-Dichloro-4-hydroxy-benzyl)-1-(4,5,6,7-tetrahydro-1H-indazol-4-yl)-pyrrolidin-2-one

HRID 1013817

反応式

C([O:8][C:9]1[CH:30]=[C:29]([Cl:31])[C:12]([CH2:13][C@@H:14]2[CH2:18][CH2:17][N:16]([CH:19]3[CH2:27][CH2:26][CH2:25][C:24]4[NH:23][N:22]=[CH:21][C:20]3=4)[C:15]2=[O:28])=[C:11]([Cl:32])[CH:10]=1)C1C=CC=CC=1>C(O)C.[OH-].[OH-].[Pd+2]>[Cl:31][C:29]1[CH:30]=[C:9]([OH:8])[CH:10]=[C:11]([Cl:32])[C:12]=1[CH2:13][C@@H:14]1[CH2:18][CH2:17][N:16]([CH:19]2[CH2:27][CH2:26][CH2:25][C:24]3[NH:23][N:22]=[CH:21][C:20]2=3)[C:15]1=[O:28]

参加物

実験手順

To a solution of (R)-3-(4-benzyloxy-2,6-dichloro-benzyl)-1-(4,5,6,7-tetrahydro-1H-indazol-4-yl)-pyrrolidin-2-one (1.32 g) in ethanol (50 mL), add palladium hydroxide on carbon (10%, 0.65 g). Stir the mixture under hydrogenation (50 psi) at room temperature for 3 hours. Filter the mixture through celite. Remove the solvent in vacuo to afford 0.93 g of the title compound. MS (m/z): 380 (M+).

後処理

filtrationFilter the mixture through celite
customRemove the solvent in vacuo

出典と根拠

ORDレコード: ord-c418ae8aa8cd4db1b1e8297e494bdd47
出典データセット: uspto-grants-2011_07
DOI: 10.6084/m9.figshare.5104873.v1
特許番号: US07981918B2

反応式

参加物

反応物 1

生成物 1

試薬・触媒・溶媒 2

実験手順

後処理

出典と根拠

関連ノート