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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1917333Generated: November 2, 2026

HCID 67490883, compound → HCID 58944935, compound

https://huagongshe.com/reaction/1917333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67490883HCID 67490883—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
ProductHCID 58944935HCID 58944935104.4%

Reaction Steps

A 10% palladium-carbon catalyst (about 50% wet, 114 mg) was added to a solution of (−)-(1R*,5S*)-3-benzyloxycarbonyl-1-(tert-butoxycarbonylamino)-3-azabicyclo[3.3.0]octane (569 mg, 1.579 mmol) in methanol (30 mL), and the mixture was stirred in a hydrogen atmosphere at room temperature for two hours. The catalyst was removed by filtration, and then the solvent was evaporated under reduced pressure to give crude 1-(tert-butoxycarbonylamino)-3-azabicyclo[3.3.0]octane (373 mg) as a colorless transparent gummy solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618094B2
Source datasetuspto-grants-2013_12
ORD IDord-6b81949802864603a0fb3d561fcfa5e8
Source noteuspto-grants-2013_12