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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444196Generated: October 27, 2026

Phosphate → N-methoxy-N-methyl-2-bromoimidazo[5,1-b]thiazole-7-carboxamide

https://huagongshe.com/reaction/1444196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphateHCID 1061—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
ReactantDiethyl aluminum chlorideHCID 16686102—
ReactantMethyl 2-bromoimidazo[5,1-b]thiazole-7-carboxylateHCID 59168410—
SolventDichloromethaneHCID 6344—
ProductN-methoxy-N-methyl-2-bromoimidazo[5,1-b]thiazole-7-carboxamideHCID 5916839888.6%

Reaction Steps

Diethylaluminum chloride (0.9 M hexane solution; 1.1 ml, 1.07 mmol) was added to an ice cooled solution of N,O-dimethylhydroxylamine hydrochloride (104 mg, 1.07 mmol) in dichloromethane (4 ml), and, while gradually raising the temperature, the mixture was stirred for one hr. A solution of methyl 2-bromoimidazo[5,1-b]thiazole-7-carboxylate (56 mg, 0.21 mmol) in dichloromethane (6 ml) was added thereto, and the mixture was stirred at room temperature for 21 hr. A phosphate buffer solution (5 ml) was added to the reaction solution, and the mixture was stirred at room temperature for 10 min and was then filtered through Celite. The filtrate was washed with saturated brine and was then dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure. The residue was purified by column chromatography on silica gel (ethyl acetate:methanol=60:1→10:1) to give N-methoxy-N-methyl-2-bromoimidazo[5,1-b]thiazole-7-carboxamide (54 mg, 88%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662841B2
Source datasetuspto-grants-2010_02
ORD IDord-51c8e1cfb68f48589fbeeda3f466929b
Source noteuspto-grants-2010_02