HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597852Generated: October 31, 2026
Methanesulfonic Acid → HCID 178458291, compound
https://huagongshe.com/reaction/1597852
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | 2-Propoxy-benzaldehyde | HCID 249807 | — |
| Reactant | 5-amino-1-tert-butyl-1H-pyrazole-4-carboxamide | HCID 21846075 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178458291 | HCID 178458291 | 22% |
Reaction Steps
A mixture of 2-propoxybenzaldehyde (3.0 g, 18.27 mmol), 1-tert-butyl-5-amino-1H-pyrazole-4-carboxamide (2.5 g, 13.7 mmol), methanesulfonic acid (0.2 ml) and xylenes (50 ml) was refluxed overnight. The reaction mixture was stripped to dryness, treated with ethanol and again stripped to dryness. The residue was partitioned between chloroform and 10% KHCO3, the layers were separated, and the aqueous layer was extracted with chloroform (2×100 ml). The organic layers were combined, and concentrated in vacuo and the residue was dissolved in CH2Cl2 (30 ml) and combined with silica gel (20 g). The preloaded silica gel was placed on a silica gel column and eluted with 70% ether/hexanes, followed by ether (100%) to afford 0.98 g (22%) of 1-tert-butyl-6-(2-propoxyphenyl)pyrazolo[3,4-d]pyrimidin-4-one 1/100 hydrate, m.p. 130°-131° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05736548 |
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| Source dataset | uspto-grants-1998_04 |
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| ORD ID | ord-1fbcb09b7981437da63b26a8d76a8493 |
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| Source note | uspto-grants-1998_04 |
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