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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880244Generated: October 31, 2026

Ethylthioacetic acid → HCID 49763423, compound

https://huagongshe.com/reaction/1880244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylthioacetic acidHCID 69387—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 86649763HCID 86649763—
SolventDichloromethaneHCID 6344—
ProductHCID 49763423HCID 49763423—

Reaction Steps

To a solution of 0.10 g of 3-[3-chloro-4-[N-(methyl)aminomethyl]phenyl]-5-(3,4,5-trichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazole and 0.038 g of (ethylthio)acetic acid in 3 mL of dichloromethane, 0.089 g of 1-[3-(dimethylamino) propyl]-3-ethylcarbodiimide hydrochloride was added and the resultant mixture was stirred at room temperature for 3 hours. After the completion of the reaction, the reaction mixture was washed with water (5 mL×1) and then dehydrated and dried over saturated saline and anhydrous sodium sulfate in this order, and then the solvent was distilled off under reduced pressure. The resultant residue was purified by preparative medium pressure liquid chromatography eluting with ethyl acetate-hexane (a gradient from 1:5 to 1:3) using a medium pressure preparative apparatus (trade name: YFLC-Wprep; manufactured by Yamazen Corporation) to obtain 0.083 g of the objective substance as a colorless resinoid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318757B2
Source datasetuspto-grants-2012_11
ORD IDord-020e4ff0f45d40278c9e75b550066678
Source noteuspto-grants-2012_11