Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783556Generated: October 30, 2026

Allylamine → N-Allyl-4-(isopropylamino)-2-(methylthio)pyrimidine-5-carboxamide

https://huagongshe.com/reaction/1783556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllylamineHCID 7853—
Reactant4-(Isopropylamino)-2-(methylthio)pyrimidine-5-carboxylic acid chlorideHCID 53963650—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductN-Allyl-4-(isopropylamino)-2-(methylthio)pyrimidine-5-carboxamideHCID 5423198251%

Reaction Steps

To a 0° C. suspension of 4-(isopropylamino)-2-(methylthio)pyrimidine-5-carboxylic acid chloride in 10 mL of tetrahydrofuran is added 3.5 mL (46.2 mmol) of allylamine and 20 mL of tetrahydrofuran. The reaction suspension is allowed to warm briefly to room temperature, then stored at 0° C. overnight. The reaction mixture is diluted with ethyl acetate, washed with 1N HCl, a saturated solution of sodium bicarbonate, and brine. The organic phase is dried over magnesium sulfate, filtered, and concentrated to give 2.1 g (51%) of the title compound:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501425B1
Source datasetuspto-grants-2009_03
ORD IDord-161ff308cde042ffb55afce2d51f1f15
Source noteuspto-grants-2009_03