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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478818Generated: October 31, 2026

Diisopropylethylamine → HCID 118513278, compound

https://huagongshe.com/reaction/1478818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-(4-METHOXY-PHENYL)-5-METHYL-1H-[1,2,3]TRIAZOLE-4-CARBOXYLIC ACIDHCID 728316—
Reactant4-amino-2-cyclohexyl-1,5-dimethyl-2,3-dihydro-1H-pyrazol-3-oneHCID 61273021—
CatalystMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 118513278HCID 118513278—

Reaction Steps

To a vial was added 1-(4-methoxyphenyl)-5-methyl-1H-1,2,3-triazole-4-carboxylic acid (0.040 g, 0.170 mmol) and a solution of Ghosez reagent (0.047 ml, 0.340 mmol) in DCM (0.95 ml). The mixture was sonicated and heated to aid dissolution. The vial was placed on the IKA shaker for 4 hours. To this mixture was added a solution of 4-amino-2-cyclohexyl-1,5-dimethyl-1H-pyrazol-3(2H)-one (Intermediate A) (10.043 g, 0.204 mmol) and N,N-diisopropylethylamine (0.030 ml, 0.170 mmol) in DCM (0.97 ml) and the vial was shaken for 16 hrs. A few drops of MeOH were added and the solvent was removed using a Genevac HT-4X evaporator. The crude mixture was purified by reverse phase chromatography and the product fraction was concentrated using a Genevac HT-4X evaporator. The crude product was dissolved in MeOH (1 ml) and eluted through a SiCO3 cartridge using MeOH as the eluent. The collected eluent was concentrated to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403833B2
Source datasetuspto-grants-2016_08
ORD IDord-64e4670566cb42feb8311a2b92818794
Source noteuspto-grants-2016_08