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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460721Generated: October 29, 2026

p-Toluenesulfonic acid monohydrate → HCID 178513505, compound

https://huagongshe.com/reaction/460721

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant3-(4-Benzyloxy-phenyl)-2-cyclohexyl-3-oxo-propionic acid methyl esterHCID 58825031—
ReactantHCID 178513689HCID 178513689—
SolventTolueneHCID 1140—
ProductHCID 178513505HCID 1785135052%

Reaction Steps

A mixture of 1.0 g (2.7 mmol) of 3-(4-benzyloxy-phenyl)-2-cyclohexyl-3-oxo-propionic acid methyl ester, 340 mg (2.7 mmol) of 5-amino-1H-pyrazole-3-carboxylic acid amide, 51 mg (10 mol %) of p-toluenesulfonic acid monohydrate (PTSA), and 15 mL of toluene was heated at reflux for 72 h. The reaction mixture was then concentrated to a residue which chromatographed on silica gel (Biotage; gradient elution 15% ethyl acetate in dichloromethane to 6% methanol in dichloromethane) to give a residue which was further purified via reverse-phase chromatography (Gilson) to afford (after lyophilization) 22 mg (2% yield) of desired 5-(4-benzyloxy-phenyl)-6-cyclohexyl-7-oxo-4,7-dihydro-pyrazolo[1,5-a]pyrimidine-2-carboxylic acid amide as indicated by 1H-NMR; LC-MS calcd for C26H26N4O3 [M++H]+: 443.2, found: 443.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196111B2
Source datasetuspto-grants-2007_03
ORD IDord-3426370c60b74365a2a331c03aef2a58
Source noteuspto-grants-2007_03