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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637623Generated: November 1, 2026

2-[(3-Chloro-2-chloromethyl-pyridin-4-yl)-methyl-amino]-ethanol → 2-{[2-(1H-benzimidazol-2-ylsulfanylmethyl)-3-chloropyridin-4-yl]-methylamino}-ethanol

https://huagongshe.com/reaction/1637623

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-[(3-Chloro-2-chloromethyl-pyridin-4-yl)-methyl-amino]-ethanolHCID 54365808—
ReactantHCID 178527775HCID 178527775—
SolventIsopropanolHCID 3776—
Product2-{[2-(1H-benzimidazol-2-ylsulfanylmethyl)-3-chloropyridin-4-yl]-methylamino}-ethanolHCID 18799391—

Reaction Conditions

Temperature4 °C

Reaction Steps

A solution of 2-[(3-chloro-2-chloromethyl-pyridin-4-yl)-methyl-amino]-ethanol isolated in step a) (10.2 g) and 2-mercapto-benzimidazole (5.8 g, 39 mmol) in 2-propanol (250 ml) is boiled under reflux for 2 h. After cooling to 4° C. the precipitate is filtered, washed with 2-propanol and dried in vacuo. The residue is dissolved in water, adjusted to pH 8 with aqueous sodium bicarbonate solution and extracted with ethyl acetate. The combined organic extracts are washed with water, dried over magnesium sulfate and evaporated in vacuo. The residue is crystallized from ethyl acetate to give the title compound as an off-white solid, 7.9 g (58%). M.p. 132-5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06043242
Source datasetuspto-grants-2000_03
ORD IDord-ff0df0e4df0e4a9ea1b073210defe7f8
Source noteuspto-grants-2000_03