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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Tetramethoxypropane | HCID 66019 | — |
| Reactant | 4-Bromo-3-phenyl-1H-pyrazol-5-amine | HCID 594319 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-Bromo-2-phenylpyrazolo[1,5-a]pyrimidine | HCID 83744419 | 76.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09023844B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-32df2614b91f4eb19b253315662d9639 |
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| Source note | uspto-grants-2015_05 |
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