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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946694Generated: October 26, 2026

Diisopropylamine → Ethyl 4-(4-(6-chloropyrimidine-4-carboxamido)-3-methylphenylsulfonamido)butanoate

https://huagongshe.com/reaction/1946694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
Reactantgamma-Aminobutyric acid ethyl esterHCID 23365—
Reactant4-(6-Chloropyrimidine-4-carboxamido)-3-methylbenzene-1-sulfonyl chlorideHCID 59446845—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-(4-(6-chloropyrimidine-4-carboxamido)-3-methylphenylsulfonamido)butanoateHCID 59446961—

Reaction Steps

A solution of 4-(6-chloropyrimidine-4-carboxamido)-3-methylbenzene-1-sulfonyl chloride (Intermediate 30, 1.2 g; 3.47 mmol) in THF (100 ml) was treated with ethyl 4-aminobutanoate (720 mg; 4.34 mmol) and diisopropylamine (2 ml; 14.3 mmol). After stirring at RT for 18 hours the solvent was removed in vacuo and the residue redissolved in DCM and washed with water. The organic extracts were passed through a hydrophobic frit and the solvent removed in vacuo. The residue was purified by column chromatography (silica) eluting with petroleum ether containing increasing amounts of EtOAc. The title product was obtained as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399448B2
Source datasetuspto-grants-2013_03
ORD IDord-fc0243b5b9d44e718f2d7231a0087e7c
Source noteuspto-grants-2013_03