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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1917352Generated: October 31, 2026

HCID 67490940, compound → HCID 67491146, compound

https://huagongshe.com/reaction/1917352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67490940HCID 67490940—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
ProductHCID 67491146HCID 6749114699.4%

Reaction Steps

{(1S,5R,6S)-1-tert-Butoxycarbonylamino-6-fluoro-3-azabicyclo[3,3,0]octan-3-yl}carboxylic acid benzyl ester (132 mg, 0.35 mmol) was dissolved in methanol (10 mL). 10% palladium-carbon (M, wet) (50 mg) was added, and the mixture was stirred in a hydrogen atmosphere for three hours. The catalyst was removed by filtration, and then the filtrate was concentrated under reduced pressure. A 1N sodium hydroxide solution was added, followed by extraction with chloroform. After drying over anhydrous sodium sulfate and filtration, the filtrate was concentrated under reduced pressure to give 85 mg of the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618094B2
Source datasetuspto-grants-2013_12
ORD IDord-ee1cb3a0f0814ea394bdd9075fb02fe8
Source noteuspto-grants-2013_12