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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588622Generated: October 30, 2026

Sodium borohydride → 2-(5-amino-3-phenyl-4-(phenylethynyl)-1H-pyrazol-1-yl)ethan-1-ol

https://huagongshe.com/reaction/588622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactantethyl 2-(5-acetamido-3-phenyl-4-(phenylethynyl)-1H-pyrazol-1-yl)acetateHCID 70983078—
SolventEthanolHCID 702—
Product2-(5-amino-3-phenyl-4-(phenylethynyl)-1H-pyrazol-1-yl)ethan-1-olHCID 8671731856.6%

Reaction Steps

To a suspension of ethyl 2-[5-acetamido-3-phenyl-4-(2-phenylethynyl)pyrazol-1-yl]acetate (22.4 g, 58 mmol) in ethanol (290 mL) was added sodium borohydride (11 g, 289 mmol) and the reaction stirred at room temperature for 16 h. The reaction mixture was partially concentrated to a final volume of 250 mL. 25% NaOH (250 mL) was added and the reaction mixture was stirred at 80° C. for 4 h. The reaction mixture was cooled down to room temperature and the two phases were separated. The aqueous phase was extracted with ethyl acetate three times and the organic phases combined, dried over MgSO4, filtered and evaporated. The residue was triturated from diethyl ether (20 mL) and the product was filtered and dried in vacuo to provide the title compound as an off-white solid (9.96 g). The mother liquor was concentrated in vacuo and purified by column chromatography (silica gel, gradient 0 to 100% ethyl acetate/isohexane) yielding a further 1.79 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227976B2
Source datasetuspto-grants-2016_01
ORD IDord-ff0b4af643514bd492c5cb2d21083bbe
Source noteuspto-grants-2016_01