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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444193Generated: November 2, 2026

Methyl morpholine oxide → 2-Bromoimidazo[5,1-b]thiazole-7-carbaldehyde

https://huagongshe.com/reaction/1444193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl morpholine oxideHCID 82029—
Reactant2-Bromo-7-hydroxymethylimidazo[5,1-b]thiazoleHCID 59168406—
CatalystHCID 178419074HCID 178419074—
SolventDichloromethaneHCID 6344—
Product2-Bromoimidazo[5,1-b]thiazole-7-carbaldehydeHCID 1152874421%

Reaction Steps

Dried 4A molecular sieves (40 mg) and tetra-n-propylammonium perruthenate (16 mg, 0.05 mmol) were added to a solution of 2-bromo-7-hydroxymethylimidazo[5,1-b]thiazole (53 mg, 0.23 mmol) and N-methylmorpholine-N-oxide (92 mg, 0.79 mmol) in dichloromethane (2 ml), and the mixture was stirred at room temperature for 3 days. The reaction solution was purified by column chromatography on silica gel (ethyl acetate:methanol=60:1) to give 2-bromoimidazo[5,1-b]thiazole-7-carbaldehyde (11 mg, 21%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662841B2
Source datasetuspto-grants-2010_02
ORD IDord-26e0f52d712142ab8df2a0f7f16a38df
Source noteuspto-grants-2010_02