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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 887174Generated: October 27, 2026

Trichloroacetyl chloride → 2,2,2-trichloro-N-isoquinolin-5-ylacetamide

https://huagongshe.com/reaction/887174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloroacetyl chlorideHCID 6420—
Reactant5-AminoisoquinolineHCID 70766—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Product2,2,2-trichloro-N-isoquinolin-5-ylacetamideHCID 889325165.1%

Reaction Steps

A solution of 5-aminoisoquinoline (1.0 g, 6.9 mmol) in dichloromethane (40 mL) and Et3N (1 mL) at 5° C. was treated with trichloroacetyl chloride (1.38 g, 7.6 mmol) dropwise. The reaction mixture was stirred at ambient temperature for 14 hours, concentrated, diluted with ethyl acetate and washed with 1N HCl. The aqueous layer was treated with aqueous NaHCO3 and extracted with ethyl acetate. The organic layer the was washed with water and concentrated. The solid residue was suspended in ethyl acetate (5 mL) and filtered to obtain 1.3 g (65%) of the title compound as a tan solid. 1H NMR (300 MHz, d6-DMSO) δ 11.20 (broad s, 1H), 9.41, (s, 1H), 8.60 (d, 1H), 8.18 (m, 1H), 7.77 (m, 2H), 7.66 (d, 1H); MS (DCI/NH3) m/z 289 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247413B2
Source datasetuspto-grants-2012_08
ORD IDord-a6b1b1df59a04ff08cb65567d59327af
Source noteuspto-grants-2012_08