Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795454Generated: October 27, 2026

Diisopropylethylamine → 2-[2-(Isopropylamino-methyl)-pyrrolidin-1-yl]-3-methyl-6-pyridin-4-yl-5-m-tolyl-3H-pyrimidin-4-one

https://huagongshe.com/reaction/1795454

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant(R)-isopropyl-pyrrolidin-2-ylmethyl-amineHCID 11564489—
Reactant2-Chloro-3-methyl-6-pyridin-4-yl-5-m-tolyl-3H-pyrimidin-4-oneHCID 16115688—
Reactant5-(3-Bromo-phenyl)-2-chloro-3-methyl-6-pyridin-4-yl-3H-pyrimidin-4-oneHCID 22185186—
SolventDichloromethaneHCID 6344—
Product2-[2-(Isopropylamino-methyl)-pyrrolidin-1-yl]-3-methyl-6-pyridin-4-yl-5-m-tolyl-3H-pyrimidin-4-oneHCID 22185211—

Reaction Steps

To a 100 mL RBF, was added (R)-isopropyl-pyrrolidin-2-ylmethyl-amine (0.13 g, 0.6 mmol), and 50 mL dichloromethane at 0° C. under nitrogen. 0.28 mL diisopropylethylamine (1.6 mmol) was added drop wise, and stirred for 10 min. 2-Chloro-3-methyl-6-pyridin-4-yl-5-m-tolyl-3H-pyrimidin-4-one (0.16 g, 0.5 mmol) was added in one portion, and stirred at 0° C. to rt for 12 h. (This meta-methyl chloro-intermediate was synthesized by a similar procedure as that of 5-(3-Bromo-phenyl)-2-chloro-3-methyl-6-pyridin-4-yl-3H-pyrimidin-4-one.) The mixture was diluted with 100 mL dichloromethane, washed with sat. NaHCO3 and brine. After purified by flash chromatography, the title compound was obtained in 0.219 g as pale yellow solid. MS (ES+): 418 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07026326B2
Source datasetuspto-grants-2006_04
ORD IDord-6ed2ec9ae5184a758d239be3ba870bb0
Source noteuspto-grants-2006_04