Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171655Generated: November 2, 2026

Hydrochloric Acid → HCID 23138536, compound

https://huagongshe.com/reaction/1171655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantHCID 23138741HCID 23138741—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 23138536HCID 2313853646%

Reaction Steps

To a solution of (E)-1-[2-cyclopropyl-1-(2-fluorophenyl)-2-oxoethyl]-3-{[1-(ethoxycarbonylmethyl)-1H-pyrazol-3-yl]methylidene}-4-sulfanylpiperidine hydrochloride (140 mg) in dichloromethane (5 ml) were added acetyl chloride (0.02 ml) and triethylamine (0.12 ml), and the resulting mixture was stirred at room temperature for 40 minutes. To the resulting reaction mixture were added acetyl chloride (0.02 ml) and triethylamine (0.4 ml), and the resulting mixture was stirred at room temperature for 80 minutes. The reaction mixture was concentrated in vacuo, and the residue was purified by chromatography on a silica gel column using methanol and dichloromethane (1:19) as the eluent. The yellow oily product obtained was dissolved in dichloromethane (3 ml) and a 4N solution of hydrogen chloride in dioxane (0.11 ml) was added to the resulting solution. After evaporation of the solvent of the reaction mixture under reduced pressure, the title compound (70 mg, yield: 46%) was afforded as a pale yellow amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829580B2
Source datasetuspto-grants-2010_11
ORD IDord-00a0900b9c6f4f77b42b515011707051
Source noteuspto-grants-2010_11