HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N'-Dimethylthiourea → 3-Methyl-2-methylimino-7-(4-trifluoromethylphenyl)-2,3,8,8a-tetrahydroindeno[1,2-d]thiazol-3a-ol hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N'-Dimethylthiourea | HCID 2723631 | — |
| Reactant | 2-Bromo-4-(4-trifluoromethylphenyl)-1-indanone | HCID 21702063 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3-Methyl-2-methylimino-7-(4-trifluoromethylphenyl)-2,3,8,8a-tetrahydroindeno[1,2-d]thiazol-3a-ol hydrobromide | HCID 20638583 | — |
| Product | 3-Methyl-2-methylimino-7-(4-trifluoromethylphenyl)-2,3,8,8a-tetrahydroindeno[1,2-d]thiazol-3a-ol | HCID 20638584 | — |
Reaction Steps
426 mg (1.2 mmol) of 2-bromo-4-(4-trifluoromethylphenyl)-1-indanone and 130.2 mg (1.25 mmol) of N,N′-dimethylthiourea are dissolved in 10 ml of acetone and stirred at room temperature for 4 h. The precipitate is filtered off with suction, washed with acetone and dried in vacuo. The hydrobromide of 3-methyl-2-methylimino-7-(4-trifluoromethylphenyl)-2,3,8,8a-tetrahydroindeno[1,2-d]thiazol-3a-ol is obtained with a melting point of 202-204° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06207689B1 |
| Source dataset | uspto-grants-2001_03 |
| ORD ID | ord-9dbe5b06f45643caa7654a4ed1bce217 |
| Source note | uspto-grants-2001_03 |