Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075791Generated: November 2, 2026

N,N-Dimethylaniline → 4-Chloro-6-cyclopentylpyrimidin-2-amine

https://huagongshe.com/reaction/2075791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant2-Amino-6-cyclopentylpyrimidin-4-OLHCID 135493693—
CatalystTetraethylammonium ChlorideHCID 5946—
SolventAcetonitrileHCID 6342—
Product4-Chloro-6-cyclopentylpyrimidin-2-amineHCID 21846367120.5%

Reaction Conditions

Temperature110 °C

Reaction Steps

A suspension of 2-amino-6-cyclopentyl-3H-pyrimidin-4-one (1.52 g, 8.4 mmol), tetraethyl ammonium chloride (2.8 g 16.9 mmol) and dimethylaniline (1.1 mL, 8.4 mmol) in acetonitrile (16 mL) was treated with phosphorous oxychloride (4.7 mL, 51 mmol) and heated at 110° C. for 20 min. The resulting solution was cooled to rt and concentrated to minimum volume then diluted with CHCl3 and ice and stirred for 30 min. The layers were separated and the organic layer was washed with water (3×50 mL) and 5% NaHCO3, dried, and concentrated to yield 2.0 g of crude product that was used without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07923451B2
Source datasetuspto-grants-2011_04
ORD IDord-fe851fcf99474699b1e8e39c01f46130
Source noteuspto-grants-2011_04