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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | N-Ethyl-N'-[7-(phenylsulfanyl)-1,3-benzothiazol-2-yl]urea | HCID 21985560 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-Ethyl-N'-[7-(phenylsulfinyl)-1,3-benzothiazol-2-yl]urea | HCID 21985603 | 38.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07091227B2 |
|---|
| Source dataset | uspto-grants-2006_08 |
|---|
| ORD ID | ord-ac6888f33d2349549c68bc6416e95d15 |
|---|
| Source note | uspto-grants-2006_08 |
|---|