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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570138Generated: October 31, 2026

Water → 3-Bromo-2-phenylpyrazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/570138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium HydroxideHCID 14923—
ReactantTetramethoxypropaneHCID 66019—
Reactant4-Bromo-3-phenyl-1H-pyrazol-5-amineHCID 594319—
SolventAcetic AcidHCID 176—
Product3-Bromo-2-phenylpyrazolo[1,5-a]pyrimidineHCID 8374441976.6%

Reaction Conditions

Temperature110 °C

Reaction Steps

To a solution of 4-bromo-3-phenyl-1H-pyrazole-5-amine (5.0 g, 0.02 mol) in acetic acid (50 mL) is added 1,1,3,3-tetramethoxypropane (4.14 g, 0.025 mol). The mixture is stirred at 110° C. for 1 h. The reaction mixture is then poured into water, basified with NH4OH and extracted with dichloromethane (3×100 mL). The organic layer is dried over anhydrous magnesium sulphate, filtered and concentrated under reduced pressure. The crude material is purified by column chromatography using silica gel in dichloromethane and ethyl acetate (1:0 to 95:5) as eluent and 4.2 g (75%) of 3-bromo-2-phenylpyrazolo[1,5-a]pyrimidine are obtained as a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09023844B2
Source datasetuspto-grants-2015_05
ORD IDord-32df2614b91f4eb19b253315662d9639
Source noteuspto-grants-2015_05