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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1072335Generated: November 2, 2026

Imidazo(4,3-b)(1,3)thiazole-7-carbaldehyde → 7-[(5-Methylthiopyridin-3-yl)hydroxymethyl]imidazo[5,1-b]thiazole

https://huagongshe.com/reaction/1072335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazo(4,3-b)(1,3)thiazole-7-carbaldehydeHCID 22390357—
Reactant3-Bromo-5-(methylthio)pyridineHCID 22390359—
ReactantHCID 178418244HCID 178418244—
Product7-[(5-Methylthiopyridin-3-yl)hydroxymethyl]imidazo[5,1-b]thiazoleHCID 2239031664%

Reaction Steps

7-[(5-Methylthiopyridin-3-yl)hydroxymethyl]imidazo-[5,1-b]thiazole (119 mg) was prepared in substantially the same manner as in step a) of Synthesis Example 5, except that 204 mg of 3-bromo-5-methylthiopyridine, 0.656 ml of a 1.6 N n-butyllithium/n-hexane solution, and 102 mg of 7-formylimidazo[5,1-b]thiazole were used as the starting materials.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06908913B2
Source datasetuspto-grants-2005_06
ORD IDord-c30938443d744290a16789e492312dee
Source noteuspto-grants-2005_06