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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455423Generated: November 2, 2026

HCID 86596880, compound → HCID 86596882, compound

https://huagongshe.com/reaction/1455423

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86596880HCID 86596880—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 86596882HCID 8659688291.1%

Reaction Steps

A solution of tert-butyl (1R,3R,4S)-4-((S)-3-benzyloxycarbonylamino-2-oxopyrrolidin-1-yl)-3-(methylsulfonylmethyl)cyclohexylcarbamate (835 mg) in MeOH (5 mL) was charged with 10% Pd/C, Degussa (800 mg). The reaction flask was evacuated and then back-filled with hydrogen; this was repeated three more times. The reaction was stirred under 1 atm of H2 for 2 h and then filtered and concentrated to afford tert-butyl (1R,3R,4S)-4-((S)-3-amino-2-oxopyrrolidin-1-yl)-3-(methylsulfonylmethyl)cyclohexylcarbamate (566 mg). MS found: (M+H)+=390.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07482335B2
Source datasetuspto-grants-2009_01
ORD IDord-2f5326e8951c4cfaa434e8e7c9f8edad
Source noteuspto-grants-2009_01