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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497508Generated: October 31, 2026

HCID 178454290, compound → HCID 178454291, compound

https://huagongshe.com/reaction/1497508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178454290HCID 178454290—
CatalystHydrochloric AcidHCID 313—
CatalystHCID 178418390HCID 178418390—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178454291HCID 17845429181%

Reaction Steps

To a solution of benzyl N-{[4-({4-[N′,N″-bis(tert-butoxycarbonyl)carbamimidamido]benzoyl}oxy)-2-chlorophenyl]acetyl}-3-fluoro-L-phenylalaninate (260 mg) in tetrahydrofuran (4.00 mL) was added one drop of 1 M hydrochloric acid, and 10% palladium-carbon (20.5 mg) was added under an argon atmosphere, followed by stirring at room temperature for 1 hour at normal pressure under a hydrogen atmosphere. The reaction mixture was filtered through Celite, and the filtrate was concentrated under reduced pressure to obtain N-{[4-({4-[N′,N″-bis(tert-butoxycarbonyl)carbamimidamido]benzoyl}oxy)-2-chlorophenyl]acetyl}-3-fluoro-L-phenylalanine (187 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199927B2
Source datasetuspto-grants-2015_12
ORD IDord-891630bb1dc341d78cfb1cc24127ef98
Source noteuspto-grants-2015_12