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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585906Generated: October 30, 2026

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

https://huagongshe.com/reaction/585906

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 numberUS06933311B2
Source datasetuspto-grants-2005_08
ORD IDord-c719ad2fa89f4e01a97a905dc55a377b
Source noteuspto-grants-2005_08