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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 3-(4-Benzyloxy-phenyl)-2-cyclohexyl-3-oxo-propionic acid methyl ester | HCID 58825031 | — |
| Reactant | HCID 178513689 | HCID 178513689 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178513505 | HCID 178513505 | 2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07196111B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-3426370c60b74365a2a331c03aef2a58 |
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| Source note | uspto-grants-2007_03 |
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