HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Chloroperbenzoic acid → 4-(7-bromo-benzooxazol-2-ylamino)-2,N,N-trimethyl-benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 4-amino-N,N,2-trimethylbenzamide | HCID 53622912 | — |
| Reactant | 7-Bromo-2-(methylthio)benzo[d]oxazole | HCID 67456811 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(7-bromo-benzooxazol-2-ylamino)-2,N,N-trimethyl-benzamide | HCID 67457821 | — |
Reaction Steps
To a solution of 0.49 g (2.01 mmol) 7-bromo-2-methylsulfanyl-benzooxazole in 30 ml dichloromethane, 3-chloroperbenzoic acid (0.494 g, 2.01 mmol) is added. This mixture is stirred for 1 h at room temperature. Then, 0.325 g (1.82 mmol) 4-amino-2,N,N-trimethyl-benzamide is added and the reaction mixture is heated to 40° C. with stirring continued for 20 h. The reaction mixture is concentrated in vacuo and the residue is purified by chromatography (silicagel, hexane:EtOAc=1:1=>1:4) to afford the title compound as an off-white crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08629168B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-5106ed6459f947d7a9e5871c155eacf2 |
| Source note | uspto-grants-2014_01 |