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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 237892Generated: October 26, 2026

2-(4-Methylcyclohexyl)acetic acid → HCID 135508420, compound

https://huagongshe.com/reaction/237892

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Methylcyclohexyl)acetic acidHCID 3616945—
Reactant5-Amino-1-(o-tolyl)-1H-pyrazole-4-carboxamideHCID 11983907—
ReactantTrimethyl(phosphooxy)silaneHCID 16133246—
SolventWaterHCID 962—
ProductHCID 135508420HCID 135508420—

Reaction Conditions

Temperature130 °C

Reaction Steps

150 mg (0.69 mmol) of 5-amino-1-(2-methylphenyl)-1H-pyrazole-4-carboxamide (Example 23A) and 130 mg (0.83 mmol) of 2-(4-methylcyclohexyl)acetic acid are mixed with 3 ml of trimethylsilyl polyphosphate and stirred at 130° C. for 3 h. The hot reaction mixture is added to 20 ml of water and then extracted with dichloromethane (2×20 ml). The combined organic phases are washed with water (20 ml) and with saturated sodium chloride solution (20 ml) and dried over sodium sulphate. The solvent is distilled off under reduced pressure, and the crude product is purified by preparative HPLC(YMC Gel ODS-AQ S 5/15 μm; eluent A: water, eluent B: acetonitrile; gradient: 0 min 30% B, 5 min 30% B, 50 min 95% B). 182 g (78% of theory) of the product are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642605B2
Source datasetuspto-grants-2014_02
ORD IDord-fc65be464776411697a6f5ca1959d8e0
Source noteuspto-grants-2014_02