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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158653Generated: October 31, 2026

Triethylamine → HCID 67327734, compound

https://huagongshe.com/reaction/1158653

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBromoacetyl chlorideHCID 89602—
Reactant6-{(SR)-1-[(3RS,4SR)-4-(3,4-Dichloro-phenyl)-pyrrolidin-3-yl]-ethoxy}-nicotinonitrileHCID 66999718—
SolventDichloromethaneHCID 6344—
ProductHCID 67327734HCID 67327734703.7%

Reaction Steps

To a stirred solution of 6-{(SR)-1-[(3RS,4SR)-4-(3,4-Dichloro-phenyl)-pyrrolidin-3-yl]-ethoxy}-nicotinonitrile (XV-B-4) 30 mg (0.083 mmol) in CH2Cl2 (3 mL) at RT, 0.013 ml (0.01 mmol) of Et3N and 0.0083 mL (0.01 mmol) of bromo-acetyl chloride were added. Stirring was continued over night and then concentrated under vacuo. The crude residue was dissolved in EtOAc, washed with H2O. The organic phase was dried over Na2SO4 and the product was purified by flash chromatography (SiO2, EtOAc) to yield the title product 34 mg (85%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812021B2
Source datasetuspto-grants-2010_10
ORD IDord-2777440fad8a498186d21e5179f3065c
Source noteuspto-grants-2010_10