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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719763Generated: October 25, 2026

Tetrahydrofuran → N-(4-(3-chloro-5-trifluoromethyl-2-pyridyloxy)-3-(1-pyrrolyl)phenyl)-2-chloro-5-nitrobenzamide

https://huagongshe.com/reaction/719763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantBenzoyl chloride, 2-chloro-5-nitro-HCID 117637—
Reactant4-(3-Chloro-5-trifluoromethyl-2-pyridyloxy)-3-(1-pyrrolyl)anilineHCID 21901882—
SolventWaterHCID 962—
ProductN-(4-(3-chloro-5-trifluoromethyl-2-pyridyloxy)-3-(1-pyrrolyl)phenyl)-2-chloro-5-nitrobenzamideHCID 1028032453.5%

Reaction Steps

To 5 mL of a tetrahydrofuran solution comprising 320 mg of 4-(3-chloro-5-trifluoromethyl-2-pyridyloxy)-3-(1-pyrrolyl)aniline and 110 mg of triethylamine, 5 mL of a tetrahydrofuran solution comprising 200 mg of 2-chloro-5-nitrobenzoylchloride was dropwise added, followed by stirring for about 30 minutes, and then water was added, and the precipitated crystals were collected by filtration. The collected crystals were washed with water and then dried to obtain 260 mg of N-(4-(3-chloro-5-trifluoromethyl-2-pyridyloxy)-3-(1-pyrrolyl)phenyl)-2-chloro-5-nitrobenzamide (Compound No. 127) having a melting point of from 165 to 167° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132546B2
Source datasetuspto-grants-2006_11
ORD IDord-871385b06bda4191b3074811150b6d83
Source noteuspto-grants-2006_11