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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534875Generated: October 30, 2026

Triethylamine → HCID 66792736, compound

https://huagongshe.com/reaction/534875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Methyl-6-nitrobenzoic anhydrideHCID 10472648—
ReactantHCID 21041395HCID 21041395—
ReactantHCID 66750856HCID 66750856—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 66792736HCID 6679273621%

Reaction Steps

A mixture of 4-[4-(2-tert-butylphenyl)piperazin-1-yl]-4-oxobutanoic acid obtained in Example 53 (500 mg), N-(cyclopropylmethyl)sulfamide (248 mg), 2-methyl-6-nitrobenzoic anhydride (692 mg), N,N-dimethylaminopyridine (192 mg), triethylamine (0.656 mL), and acetonitrile (10 mL) was stirred at room temperature for over-night. Water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to provide the title compound (148 mg, 21%) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853215B2
Source datasetuspto-grants-2014_10
ORD IDord-308fc3814ace4c45b19f40e6bdf8573d
Source noteuspto-grants-2014_10