Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2056793Generated: October 30, 2026

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

https://huagongshe.com/reaction/2056793

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), 7.77 (d, 1H); MS (DCI/NH3) m/z 289 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07335678B2
Source datasetuspto-grants-2008_02
ORD IDord-f174fcfbbc7c4f89a33e223cf01b289f
Source noteuspto-grants-2008_02