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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871023Generated: October 30, 2026

3-(Trifluoromethyl)benzoyl chloride → HCID 71621926, compound

https://huagongshe.com/reaction/871023

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)benzoyl chlorideHCID 75257—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 86689233HCID 86689233—
SolventDichloromethaneHCID 6344—
ProductHCID 71621926HCID 7162192670.3%

Reaction Steps

To a mixture of 5-amino-3-(3-aminophenyl)isothiazole-4-carboxamide (13 mg, 0.056 mmol) and N,N-diisopropylethylamine (0.029 mL, 0.17 mmol) in 1.0 mL CH2Cl2 at room temperature was added 3-(trifluoromethyl)benzoyl chloride (0.008 mL, 0.056 mmol) and the reaction stirred at room temperature. After 1 hour, additional 3-(trifluoromethyl)benzoyl chloride (0.0015 mL) was added, then again at 2 hours (0.002 mL) and 3 hours (0.0015 mL). After 4 hours the reaction was evaporated, and then treated to an aqueous Na2CO3 and EtOAc workup to yield a light yellow solid. The solid was precipitated from EtOAc/hexane to give the title compound as an off-white solid (16 mg, 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969583B2
Source datasetuspto-grants-2015_03
ORD IDord-34330f53ccb54148969987e7d49ff692
Source noteuspto-grants-2015_03