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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695988Generated: November 3, 2026

Acetone → 2,4-dichloro-N-isopropylpyrimidin-5-amine

https://huagongshe.com/reaction/1695988

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
Reactant5-Amino-2,4-dichloropyrimidineHCID 257797—
ReactantSodium cyanoborohydrideHCID 5003444—
CatalystTitanium TetrachlorideHCID 24193—
SolventDichloromethaneHCID 6344—
Product2,4-dichloro-N-isopropylpyrimidin-5-amineHCID 8665156974.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

In a 100 mL flask containing 2,4-dichloropyrimidin-5-amine (1.0 g, 6.10 mmol) in 16.5 mL of dichloromethane was added acetone (1.062 g, 18.29 mmol). The solution was cooled to 0° C. then a solution of titanium tetrachloride (0.740 mL, 6.71 mmol) in 10 mL of dichloromethane was added slowly. The mixture was stirred at room temperature for 2 hours. Sodium cyanoborohydride (1.150 g, 18.29 mmol) was added in 4 equal portions over 10 minutes and the reaction was stirred at room temperature for 2 hours. The reaction was quenched with water (150 mL) and extracted with t-BuOMe twice. The organic layers were combined, dried with Na2SO4, filtered and concentrated in vacuo. The residue was dissolved in methanol and adsorbed onto silica. The residue was purified on silica gel using 0-10% methanol in dichloromethane as eluent. Relevant fractions were evaporated in vacuo to give 940 mg (74%) of 2,4-dichloro-N-isopropylpyrimidin-5-amine as a pale yellow oil. MS [M+H] Found 206.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163755B2
Source datasetuspto-grants-2012_04
ORD IDord-12cb5bee8afc477a892fcde54e16eb9f
Source noteuspto-grants-2012_04