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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712282Generated: October 29, 2026

Boron tribromide → N-ethyl-2-(ethylcarbamoylamino)-5-hydroxy-1,3-benzothiazole-7-carboxamide

https://huagongshe.com/reaction/712282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantN-ethyl-2-(ethylcarbamoylamino)-5-methoxy-1,3-benzothiazole-7-carboxamideHCID 86663994—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductN-ethyl-2-(ethylcarbamoylamino)-5-hydroxy-1,3-benzothiazole-7-carboxamideHCID 8666399531%

Reaction Steps

Boron tribromide (8.72 mL, 8.72 mmol, 4M solution in DCM was added to a suspension of N-ethyl-2-(ethylcarbamoylamino)-5-methoxy-1,3-benzothiazole-7-carboxamide in dichloromethane (10 mL). The reaction was stirred at ambient temperature overnight then diluted with EtOAc, washed with saturated aqueous sodium hydrogen carbonate and brine and the organic layer dried (MgSO4), filtered and concentrated in vacuo. The crude material was purified by flash chromatography on silica gel using DCM:MeOH 95:5. The product was obtained as a white solid, 212 mg, 31% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181234B2
Source datasetuspto-grants-2015_11
ORD IDord-ff4aa71a21dc4d7b96b4093ad8a8712d
Source noteuspto-grants-2015_11