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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444197Generated: November 1, 2026

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

https://huagongshe.com/reaction/1444197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphateHCID 1061—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
ReactantDiethyl aluminum chlorideHCID 16686102—
ReactantEthyl 2-bromoimidazo[5,1-b]thiazole-7-carboxylateHCID 59168405—
SolventDichloromethaneHCID 6344—
ProductN-methoxy-N-methyl-2-bromoimidazo[5,1-b]thiazole-7-carboxamideHCID 5916839892.7%

Reaction Steps

Diethylaluminum chloride (0.9 M hexane solution; 2.3 ml, 2.11 mmol) was added to an ice cooled solution of N,O-dimethylhydroxylamine hydrochloride (206 mg, 2.11 mmol) in dichloromethane (8 ml), and, while gradually raising the temperature, the mixture was stirred for one hr. A solution of ethyl 2-bromoimidazo[5,1-b]thiazole-7-carboxylate (116 mg, 0.42 mmol) in dichloromethane (4 ml) was added and stirred at room temperature for 15 hr. A phosphate buffer solution (10 ml) was added to the reaction solution, and the mixture was stirred at room temperature for 10 min and was filtered through Celite. The filtrate was washed with saturated brine and was then dried over anhydrous sodium sulfate, and the solvent was removed by distillation under the reduced pressure. The residue was purified by column chromatography on silica gel (ethyl acetate:methanol=30:1→10:1) to give N-methoxy-N-methyl-2-bromoimidazo[5,1-b]thiazole-7-carboxamide (113 mg, 92%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662841B2
Source datasetuspto-grants-2010_02
ORD IDord-28d3e3d5dad04d23835b2a82ba164087
Source noteuspto-grants-2010_02