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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951135Generated: November 3, 2026

3-Chloro-2-fluoro-1-propene → N-{(3RS,4SR)-4-(3,4-Dichloro-phenyl)-1-[1-(2-fluoro-allyl)-piperidine-4-carbonyl]-pyrrolidin-3-yl}-4-methoxy-N-methyl-3-trifluoromethyl-benzamide

https://huagongshe.com/reaction/1951135

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-2-fluoro-1-propeneHCID 80320—
ReactantN-[(3RS,4SR)-4-(3,4-dichloro-phenyl)-1-(piperidine-4-carbonyl)-pyrrolidin-3-yl]-4-methoxy-N-methyl-3-trifluoromethyl-benzamideHCID 67025720—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductN-{(3RS,4SR)-4-(3,4-Dichloro-phenyl)-1-[1-(2-fluoro-allyl)-piperidine-4-carbonyl]-pyrrolidin-3-yl}-4-methoxy-N-methyl-3-trifluoromethyl-benzamideHCID 7504752047%

Reaction Steps

To a solution of N-[(3RS,4SR)-4-(3,4-dichloro-phenyl)-1-(piperidine-4-carbonyl)-pyrrolidin-3-yl]-4-methoxy-N-methyl-3-trifluoromethyl-benzamide (50 mg, 0.090 mmol) in THF (1 mL) was added under an atmosphere of nitrogen potassium bis(trimethylsilyl)amide (0.885 M in THF, 132 μL, 0.116 mmol). After stirring for 15 min at ambient temperature 3-chloro-2-fluoroprop-1-ene (13 mg, 0.13 mmol) was added and the reaction mixture was stirred for 20 h at this temperature. It was diluted with ethyl acetate (10 mL) and washed with an aqueous solution of sodium carbonate (1 M, 10 mL) and brine (10 mL). The aqueous layers were extracted with ethyl acetate (10 mL) and the combined organic layers dried over sodium sulfate. Purification by chromatography (SiO2, ethyl acetate:(ethyl acetate:triethylamine=95:5):methanol=100:0:0 to 0:90:10) afforded the title compound (26 mg, 47%) as a light brown foam. MS m/e: 616.4 [M]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404679B2
Source datasetuspto-grants-2013_03
ORD IDord-675ff178df944c7ca3dc46a5dac922e0
Source noteuspto-grants-2013_03