HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 2-(2-Ethylsulfanylphenyl)-7-trifluoromethylquinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | 4-Amino-2-(2-ethylsulfanylphenyl)-7-trifluoromethylquinazoline | HCID 118205828 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(2-Ethylsulfanylphenyl)-7-trifluoromethylquinazoline | HCID 118035584 | 15.3% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
324 mg of t-butyl nitrite was added to a mixture of 506 mg of 4-amino-2-(2-ethylsulfanylphenyl)-7-trifluoromethylquinazoline and 10 ml of DMF at 100° C., and the mixture was stirred at 100° C. for 45 minutes. Water was added to the cooled reaction mixture, and the mixture was extracted with t-butyl methyl ether. The organic layer was washed with water and dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The resulting residue was applied to a silica gel column chromatography to obtain 74 mg of 2-(2-ethylsulfanylphenyl)-7-trifluoromethylquinazoline (Compound of Present Invention 11).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09260436B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-3430edea6c204874abf4eef373b56665 |
| Source note | uspto-grants-2016_02 |