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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597852Generated: October 31, 2026

Methanesulfonic Acid → HCID 178458291, compound

https://huagongshe.com/reaction/1597852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
Reactant2-Propoxy-benzaldehydeHCID 249807—
Reactant5-amino-1-tert-butyl-1H-pyrazole-4-carboxamideHCID 21846075—
SolventEthanolHCID 702—
ProductHCID 178458291HCID 17845829122%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05736548
Source datasetuspto-grants-1998_04
ORD IDord-1fbcb09b7981437da63b26a8d76a8493
Source noteuspto-grants-1998_04