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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171656Generated: November 2, 2026

Ammonia → HCID 86609421, compound

https://huagongshe.com/reaction/1171656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantIsobutyl chloroformateHCID 62365—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86609418HCID 86609418—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 86609421HCID 8660942142%

Reaction Steps

To a solution of (E)-4-(acetylsulfanyl)-3-{[1-(carboxymethyl)-1H-pyrazol-3-yl]methylidene}-1-[2-cyclopropyl-1-(2-fluorophenyl)-2-oxoethyl]piperidine hydrochloride (190 mg) in dichloromethane (15 ml) were added isobutyl chloroformate (0.06 ml) and triethylamine (0.18 ml) under ice-cooling, and the resulting mixture was stirred at the same temperature for 30 minutes. To this reaction mixture was added 28% aqueous ammonia solution (0.03 ml), and the resulting mixture was stirred at room temperature for 45 minutes. After stirring, saturated aqueous sodium hydrogencarbonate solution was added to the reaction mixture and extracted with dichloromethane. The extract was dried over anhydrous magnesium sulfate. The solvent was removed in vacuo, and the residue was purified by chromatography on a silica gel column using a mixed solvent of methanol and dichloromethane (1:19) as the eluent to afford the title compound (80 mg, yield: 42%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829580B2
Source datasetuspto-grants-2010_11
ORD IDord-698c3f924c17434b8b7d535ad0ada377
Source noteuspto-grants-2010_11