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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9161Generated: October 28, 2026

m-Chloroperbenzoic acid → N-Ethyl-N'-[7-(phenylsulfinyl)-1,3-benzothiazol-2-yl]urea

https://huagongshe.com/reaction/9161

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantN-Ethyl-N'-[7-(phenylsulfanyl)-1,3-benzothiazol-2-yl]ureaHCID 21985560—
SolventDichloromethaneHCID 6344—
ProductN-Ethyl-N'-[7-(phenylsulfinyl)-1,3-benzothiazol-2-yl]ureaHCID 2198560338.6%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a suspension of N-ethyl-N′-[7-(phenylsulfanyl)-1,3-benzothiazol-2-yl]urea (107 mg, 0.32 mmol) in CH2Cl2 (5 mL) was added MCPBA (60 mg, 0.24 mmol, 70%). The reaction mixture was stirred at about 20° C. for about 1.5 hrs. The reaction mixture was then concentrated in vacuo. The crude reaction mixture was purified by flash chromatography on SiO2 (EtOAc/CH2Cl2 10/90). 32 mg (29%) of pure product was isolated. LC/MS 346 (MH+); RP-HPLC RT 12.96 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091227B2
Source datasetuspto-grants-2006_08
ORD IDord-ac6888f33d2349549c68bc6416e95d15
Source noteuspto-grants-2006_08