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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20847Generated: October 26, 2026

Hydrochloric Acid → (+/-)-2-Chloro-N-[{1-[(cyclopropylmethyl)(methyl)amino]cyclopentyl}(phenyl)methyl]-3-(trifluoromethyl)benzamide hydrochloride

https://huagongshe.com/reaction/20847

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantCyclopropanecarboxaldehydeHCID 123114—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant(+/-)-2-Chloro-N-[[1-(methylamino)cyclopentyl](phenyl)methyl]-3-(trifluoromethyl)benzamideHCID 59347824—
CatalystAcetic AcidHCID 176—
Solvent1,2-DichloroethaneHCID 11—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Product(+/-)-2-Chloro-N-[{1-[(cyclopropylmethyl)(methyl)amino]cyclopentyl}(phenyl)methyl]-3-(trifluoromethyl)benzamide hydrochlorideHCID 68563672—

Reaction Steps

To a solution (±)-2-chloro-N-[[1-(methylamino)cyclopentyl](phenyl)methyl]-3-(trifluoromethyl)benzamide E22 (143 g; 0.35 mmol), cyclopropanecarboxaldehyde (0.026 ml; 0.035 mmol) and acetic acid (3 drops) in 1,2-dichloroethane (10 ml) was added sodium triacetoxyborohydride (303 mg; 1.4 mmol). The resulting mixture was allowed to stir at room temperature under argon overnight. Then the reaction mixture was diluted with DCM (20 ml), washed with saturated potassium carbonate solution and brine, dried (Na2SO4) and evaporated in vacuo. The mixture was separated by column chromatography on silica gel using 20% ether in n-pentane to 2% methanol in ether. The oil obtained was treated with 1M HCl in ether to give the title product as an off white hydrochloride salt (0.054 g; 33%). Mass Spectrum (Electrospray LC/MS). Found 465 (MH+). C25H2835ClF3N2O requires 464. Ret. time: 2.30 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745642B2
Source datasetuspto-grants-2010_06
ORD IDord-bb50d10ebc9c4dcabf14fd48f8eff140
Source noteuspto-grants-2010_06