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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712289Generated: October 30, 2026

Methanesulfonic Acid → 1-ethyl-3-[5-hydroxy-7-[(E)-N-methoxy-C-methylcarbonimidoyl]-1,3-benzothiazol-2-yl]urea

https://huagongshe.com/reaction/712289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
Reactant1-ethyl-3-[7-[(E)-N-methoxy-C-methylcarbonimidoyl]-5-phenylmethoxy-1,3-benzothiazol-2-yl]ureaHCID 87222549—
SolventDichloromethaneHCID 6344—
Product1-ethyl-3-[5-hydroxy-7-[(E)-N-methoxy-C-methylcarbonimidoyl]-1,3-benzothiazol-2-yl]ureaHCID 8722246154%

Reaction Steps

A solution of methanesulfonic acid (6.5 mL) in DCM (32 mL) was added to 1-[5-benzyloxy-7-[(E)-N-methoxy-C-methyl-carbonimidoyl]-1,3-benzothiazol-2-yl]-3-ethyl-urea (718 mg, 1.8 mmol) and the reaction stirred at ambient temperature for 2 h after which time LCMS indicated clean conversion to the desired product. The reaction was diluted with DCM, washed with water and the aqueous layer neutralized with saturated aqueous Na2CO3 solution and extracted with EtOAc. The organic layer was dried (MgSO4), filtered and the solvent was removed in vacuo. The crude material obtained was purified by flash chromatography on silica gel using MeOH:DCM 3:97 as the eluent to give the desired compound as an off white solid, 300 mg, 54% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181234B2
Source datasetuspto-grants-2015_11
ORD IDord-8515c633a7964ccabdc53f7d2ab71c74
Source noteuspto-grants-2015_11