Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 527463Generated: October 30, 2026

Triethylamine → (R)-2,6-dichloro-5-methyl-N-(tetrahydrofuran-3-yl)pyrimidin-4-amine

https://huagongshe.com/reaction/527463

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,4,6-Trichloro-5-methylpyrimidineHCID 232789—
Reactant(3R)-3-Aminotetrahydrofuran hydrochlorideHCID 46856371—
SolventEthanolHCID 702—
Product(R)-2,6-dichloro-5-methyl-N-(tetrahydrofuran-3-yl)pyrimidin-4-amineHCID 9042623354.8%

Reaction Steps

A mixture of 2,4,6-trichloro-5-methylpyrimidine (2 g, 10.2 mmol), (R)-tetrahydrofuran-3-amine hydrochloride (1.12 g, 9.2 mmol) and Et3N (2.1 g, 20.3 mmol) in EtOH (20 mL) was stirred at room temperature for 14 h., concentrated under vacuum and the residue was purified by chromatographic column on silica gel (EtOAc/petroleum ether, gradient elution, from 1/0 to 2/1) to give the (R)-2,6-dichloro-5-methyl-N-(tetrahydrofuran-3-yl)pyrimidin-4-amine (1.25 g, 53% yield) as a white solid. ESI-LCMS (m/z): 248.1 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346802B2
Source datasetuspto-grants-2016_05
ORD IDord-772f106915e948ccb144b2c781f961a0
Source noteuspto-grants-2016_05