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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 583410Generated: October 31, 2026

Triethylamine → HCID 86754324, compound

https://huagongshe.com/reaction/583410

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Chloro-p-toluidineHCID 12007—
ReactantHCID 21310531HCID 21310531—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 86754324HCID 86754324—

Reaction Steps

160 mg (0.268 mmol) of 5-[N-(3,5-bistrifluoromethyl-benzoyl)-N-methyl-amino]-6-(1H-indol-3-yl)-hexanoic acid are dissolved in 10 ml of methylene chloride, and then 222 ml (1.34 mmol) of triethylamine, 48 ml (0.382 mmol) of 2-chloro-4-methyl-aniline and 271 ml of 50% propylphosphonic acid anhydride solution in ethyl acetate are added. The reaction mixture is stirred at room temperature for 20 hours, then washed twice with aqueous potassium carbonate solution. The aqueous phase is extracted twice with methylene chloride, and the organic phases are combined, dried over magnesium sulfate and concentrated by evaporation. The residue is chromatographed on silica gel with ethyl acetate/petroleum ether (first 1:2, then 3:1). The title compound is obtained in the form of white crystals. MS (EI): 352, 241, 222, 213, 130. TLC: ethyl acetate, Rf =0.59.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05929067
Source datasetuspto-grants-1999_07
ORD IDord-17a366bf80c44c75858004fc12225bf9
Source noteuspto-grants-1999_07