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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637752Generated: October 29, 2026

Water → 6-Chloro-2-[1-(3-isoquinolyl)ethylsulfanyl]pyrimidin-4-amine

https://huagongshe.com/reaction/1637752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant3-(1-Chloroethyl)-isoquinolineHCID 18799831—
ReactantHCID 178505342HCID 178505342—
SolventDimethylformamideHCID 6228—
Product6-Chloro-2-[1-(3-isoquinolyl)ethylsulfanyl]pyrimidin-4-amineHCID 49275357.3%

Reaction Steps

4-Amino-6-chloro-2-mercapto-pyrimidine mesylate salt (1.79 g, 6.94 mmole) is dissolved in 12 ml dry dimethylformamide in a 50 ml one neck round bottom flask under nitrogen. The solution is treated with 60% sodium hydride (605 mg, 15.1 mmole) (exotherm) and the mixture is stirred one hour. 3-(1-chloroethyl)-isoquinoline (1.33 g, 6.94 mmole) in 2×3 ml dry dimethylformamide, is added to the reaction and the mixture is stirred 6 hours at room temperature. The reaction mixture is poured into 300 ml water and is extracted with 3×100 ml ethyl acetate. The combined organics are backwashed with 4×50 ml 50% saturated sodium chloride. The organics are dried over potassium carbonate and are concentrated in vacuo to a yellow oil. The crude material is chromatographed over 75 g silica gel (230-400 mesh), eluting with 40% acetone/hexane while collecting 9 ml fractions. Fractions 26-39 are combined and concentrated to afford 1.26 g (57%) of 4-Amino-6-chloro-2-(1-(3-isoquinolyl)ethyl)thio-pyrimidine as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06043248
Source datasetuspto-grants-2000_03
ORD IDord-3ac6256bb5b24b3c83930ac3b8ec5af4
Source noteuspto-grants-2000_03