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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1475658Generated: October 31, 2026

(+/-)-tert-Butyl 1-[3-({cyclopentyl[4-(2,2-difluorovinyl)phenyl]acetyl}amino)benzyl]cyclopropanecarboxylate → (+/-)-tert-Butyl 1-[3-({cyclopentyl[4-(2,2-difluoroethyl)phenyl]acetyl}amino)benzyl]cyclopropanecarboxylate

https://huagongshe.com/reaction/1475658

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(+/-)-tert-Butyl 1-[3-({cyclopentyl[4-(2,2-difluorovinyl)phenyl]acetyl}amino)benzyl]cyclopropanecarboxylateHCID 66563353—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product(+/-)-tert-Butyl 1-[3-({cyclopentyl[4-(2,2-difluoroethyl)phenyl]acetyl}amino)benzyl]cyclopropanecarboxylateHCID 68170306—

Reaction Steps

100 mg of Pd/C (10%) were added to a solution of 200.0 mg (0.404 mmol) of (+/−)-tert-butyl 1-[3-({cyclopentyl[4-(2,2-difluorovinyl)phenyl]acetyl}amino)benzyl]cyclopropanecarboxylate in 5 ml of ethanol. Under atmospheric pressure, the mixture was stirred vigorously under an atmosphere of hydrogen overnight. The reaction was then filtered off through Celite and the filtrate was concentrated under reduced pressure. The crude product was purified by preparative RP-HPLC (mobile phase acetonitrile/water). This gave 151.1 mg (75.2% of theory) of the target compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018258B2
Source datasetuspto-grants-2015_04
ORD IDord-cecdabd261e44ef5ae341d1939050c08
Source noteuspto-grants-2015_04