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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576962Generated: October 26, 2026

Triethylamine → HCID 178429444, compound

https://huagongshe.com/reaction/576962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-(Bromomethyl)-2-chloropyridineHCID 18931028—
ReactantHCID 178429541HCID 178429541—
SolventEthanolHCID 702—
ProductHCID 178429444HCID 17842944454.8%

Reaction Steps

A mixture of 3-(bromomethyl)-2-chloropyridine (1.0 g, 4.8 mmol), 6-methyl-2-sulfanylpyrimidin-4-ol (570 mg, 4.0 mmol), and triethylamine (1.4 mL, 10.0 mmol) in absolute ethanol (20 mL) was stirred at room temperature overnight. The product was recovered by filtration, washed with EtOH (15 mL), diethyl ether (3×15 mL), water (3×30 mL), and hexanes (3×15 mL). The solid material was dried in vacuo, affording the 2-{[(2-chloropyridin-3-yl)methyl]sulfanyl}-6-methylpyrimidin-4-ol (400 mg, 31% yield). The product was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040538B2
Source datasetuspto-grants-2015_05
ORD IDord-76a04cb448c6470f9b96e0cfbc4c81dd
Source noteuspto-grants-2015_05