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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946693Generated: October 26, 2026

Diisopropylamine → Tert-butyl 3-(4-(6-chloropyrimidine-4-carboxamido)-3-methylphenylsulfonamido)propanoate

https://huagongshe.com/reaction/1946693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantTert-butyl 3-aminopropanoate hydrochlorideHCID 16218890—
Reactant4-(6-Chloropyrimidine-4-carboxamido)-3-methylbenzene-1-sulfonyl chlorideHCID 59446845—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 3-(4-(6-chloropyrimidine-4-carboxamido)-3-methylphenylsulfonamido)propanoateHCID 59447084—

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 tert-butyl 3-aminopropanoate hydrochloride (800 mg; 4.4 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-34aede211cb44b38862be2450cec461b
Source noteuspto-grants-2013_03