HCID 86596905, compound → HCID 68768989, compound

HRID 1374366Notes

Reaction equation

HRID 1374366 reaction equation
[CH:1]([O:4][C@@H:5]1[CH2:10][CH2:9][C@H:8]([N:11]2[CH2:15][CH2:14][C@H:13]([NH:16]C(=O)OCC3C=CC=CC=3)[C:12]2=[O:27])[C@H:7]([CH2:28][S:29]([CH:32]([CH3:34])[CH3:33])(=[O:31])=[O:30])[CH2:6]1)([CH3:3])[CH3:2].[H][H]>CO.[Pd]>[NH2:16][C@H:13]1[CH2:14][CH2:15][N:11]([C@H:8]2[CH2:9][CH2:10][C@@H:5]([O:4][CH:1]([CH3:3])[CH3:2])[CH2:6][C@H:7]2[CH2:28][S:29]([CH:32]([CH3:34])[CH3:33])(=[O:31])=[O:30])[C:12]1=[O:27]

Participants

5

Reactant 2

HCID 86596905HCID 86596905, compoundHCID 178418361HCID 178418361, compound

Product 1

HCID 68768989HCID 68768989, compound

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 887MethanolSolvent

Procedure

A sample of benzyl (S)-1-((1S,2R,4R)-4-isopropoxy-2-(isopropylsulfonylmethyl)cyclohexyl)-2-oxopyrrolidin-3-ylcarbamate A (faster ismer, 0.41 g) and Pd/C (0.08 g) were taken in MeOH (20 mL) and stirred at rt under 50 psi hydrogen pressure. After stirring overnight, the reaction mixture was filtered through Celite using EtOAc. Upon concentration and drying in vacuo, (S)-3-amino-1-((1S,2R,4R)-4-isopropoxy-2-(isopropylsulfonylmethyl)cyclohexyl)pyrrolidin-2-one was obtained as a clear viscous oil.

Workup

  1. filtrationthe reaction mixture was filtered through Celite
  2. concentrationUpon concentration
  3. customdrying in vacuo

Sources & evidence

ORD record
ord-bf8ae2b433f549e7a3601c8eb44f1a62
Source dataset
uspto-grants-2007_01
Patent number
US07163937B2

Reaction notes

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