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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917327Generated: November 1, 2026

3-Pyridinemethanol → HCID 23032463, compound

https://huagongshe.com/reaction/917327

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-PyridinemethanolHCID 7510—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant5-Chloro-3-(methylsulfanyl)-1,2,4-thiadiazoleHCID 570953—
SolventDimethylformamideHCID 6228—
ProductHCID 23032463HCID 2303246365.7%

Reaction Steps

Into 2 ml of N,N-dimethylformamide were dissolved 100 mg of 5-chloro-3-methylthio-1,2,4-thiadiazole and 78 mg of 3-pyridinemethanol, 78 mg of sodium hydride (60% in oil) was added thereto under ice-cooling, and the reaction mixture was stirred for 0.5 hour under ice-cooling and for 1 hours at room temperature. The reaction mixture was added to saturated ammonium chloride aqueous solution, and extracted with t-butyl methyl ether. The organic layer was concentrated, and the residue obtained was subjected to silica gel column chromatography to give 88 mg of 5-(3-pyridylmethyl)-3-methylthio-1,2,4-thiadiazole (hereinafter, referred to as the present compound (20)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07273879B2
Source datasetuspto-grants-2007_09
ORD IDord-b594c35055bc4a809cb0f85bf1d9726c
Source noteuspto-grants-2007_09