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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1528524Generated: October 26, 2026

Triethylamine → HCID 68745534, compound

https://huagongshe.com/reaction/1528524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-ChlorostyreneHCID 14906—
ReactantSodium HypochloriteHCID 23665760—
Reactant4-[4-[(hydroxyimino)methyl]-2-thiazolyl]-1-[[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]acetyl]piperidineHCID 86631243—
SolventDichloromethaneHCID 6344—
ProductHCID 68745534HCID 68745534—

Reaction Steps

To a solution of 1-chloro-2-ethenylbenzene (0.035 g, 0.25 mmol), triethylamine (2.5 mg, 0.025 mmol) and Clorox® aqueous sodium hypochlorite solution (1 mL, 16.1 mmol) in dichloromethane (5 mL) was added 4-[4-[(hydroxyimino)methyl]-2-thiazolyl]-1-[[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]acetyl]piperidine (i.e. the product of Example 2, Step C) (0.10 g, 0.25 mmol) in dichloromethane (5 mL) dropwise over 1 h at 0° C. The reaction mixture was allowed to stir for 1 h, then filtered through Celite® diatomaceous filter aid, and concentrated under reduced pressure to give an oil, which was purified by column chromatography on silica gel using 50% ethyl acetate in hexane as eluant to give 73 mg of the title compound as a white foam, melting at 115-122° C. (crystallized from methyl acetate/petroleum ether).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090604B2
Source datasetuspto-grants-2015_07
ORD IDord-b5b7cab993e24ba3902f6ce5b6cbf6ab
Source noteuspto-grants-2015_07