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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171579Generated: November 1, 2026

HCID 21074848, compound → HCID 68767021, compound

https://huagongshe.com/reaction/1171579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 21074848HCID 21074848—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 68767021HCID 6876702197%

Reaction Steps

A solution of (1R,2S,5R)-methyl 2-((S)-3-(benzyloxycarbonylamino)-2-oxopyrrolidin-1-yl)-5-(tert-butylamino)-cyclohexanecarboxylate (2.42 g, 5.43 mmol) in methanol was treated with 600 mg of 10% Pd/C and hydrogenated at 55 psi of H2 in a Parr shaker overnight. The catalyst was filtered and the filtrate concentrated in vacuo to give 1.64 g of (1R,2S,5R)-methyl 2-((S)-3-amino-2-oxopyrrolidin-1-yl)-5-(tert-butylamino)-cyclohexanecarboxylate as a white solid. This was used without further purification. MS found: (M+H)+=312.32.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829571B2
Source datasetuspto-grants-2010_11
ORD IDord-193d1c0084dd4ac8875e8ce00ad9aa3d
Source noteuspto-grants-2010_11