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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399974Generated: November 4, 2026

Formaldehyde → 1-[5-Bromo-6-hydroxy-7-(morpholinomethyl)-1,3-benzothiazol-2-yl]-3-ethyl-urea

https://huagongshe.com/reaction/1399974

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantMorpholineHCID 8083—
ReactantEthyl AcetateHCID 8857—
Reactant1-(5-Bromo-6-methoxy-1,3-benzothiazol-2-yl)-3-ethyl-ureaHCID 59603085—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-[5-Bromo-6-hydroxy-7-(morpholinomethyl)-1,3-benzothiazol-2-yl]-3-ethyl-ureaHCID 8669689411%

Reaction Steps

Paraformaldehyde (29 mg, 0.05 mmol) was suspended in anhydrous DMF (2 mL) under argon and morpholine (0.08 mL, 0.95 mmol) added. The mixture was stirred at RT for 10 min then Intermediate 6 (200 mg, 0.63 mmol) added. The mixture was stirred at RT overnight, heated to 90° C. for 2 h then cooled to RT. The mixture was diluted with H2O and a precipitate formed. EtOAc was added but the precipitate remained insoluble. The suspension was filtered through a PTFE filter and the solid rinsed with H2O and EtOAc. The biphasic filtrate was extracted into EtOAc (4×20 mL). The combined organic layers were washed with H2O (3×50 mL), dried (Na2SO4) and concentrated in vacuo. The material was purified by chromatography, on silica eluting with 0-10% MeOH in DCM to give Intermediate 12 (28 mg, 11%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906902B2
Source datasetuspto-grants-2014_12
ORD IDord-2507912c839e40edb7768dfd98ea6638
Source noteuspto-grants-2014_12