Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723608Generated: October 29, 2026

Triethylamine → n-{2-[4-(3,5-Dichlorobenzyl)-3,5-diethyl-1h-pyrazol-1-yl]ethyl}-2,4-dioxo-1,2,3,4-tetrahydro-5-pyrimidinesulfonamide

https://huagongshe.com/reaction/723608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,4-Dioxo-1,2,3,4-tetrahydropyrimidine-5-sulfonyl chlorideHCID 234620—
Reactant2-[4-(3,5-Dichlorobenzyl)-3,5-diethyl-1h-pyrazol-1-yl]ethanamineHCID 9923357—
SolventDimethylformamideHCID 6228—
Productn-{2-[4-(3,5-Dichlorobenzyl)-3,5-diethyl-1h-pyrazol-1-yl]ethyl}-2,4-dioxo-1,2,3,4-tetrahydro-5-pyrimidinesulfonamideHCID 10278640—

Reaction Steps

A solution of the amine of Example 43 (6.5 mg, 20 μmol) and triethylamine (6 μl, 40 μmol) in dimethylformamide (250 μL) was treated with 2,4-dioxo-1,2,3,4-tetrahydro-5-pyrimidinesulfonyl chloride (J. Am. Chem. Soc., 1956, 78, 401) (0.8 mg, 4.0 μmol) and the mixture was shaken for 18 hours. The reaction mixture was filtered and the filtrate was purified by HPLC (Hypersil Thermoquest Luna C8 150×10 mm column; a gradient mobile phase was used, 10:90 (by volume)→95:5 (by volume) acetonitrile:(water, 95% by volume/trifluoroacetic acid, 0.1% by volume/acetonitrile 5%, by volume)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141585B2
Source datasetuspto-grants-2006_11
ORD IDord-6892799b018f40609c681171d027aa03
Source noteuspto-grants-2006_11