HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylthiourea → 8b-hydroxy-2-(methylamino)-3a,4-dihydroindeno[1,2-d][1,3]thiazole-6-carbonitrile;hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylthiourea | HCID 2723704 | — |
| Reactant | 2-Bromo-1-oxoindan-5-carbonitrile | HCID 18407238 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 8b-hydroxy-2-(methylamino)-3a,4-dihydroindeno[1,2-d][1,3]thiazole-6-carbonitrile;hydrobromide | HCID 178419590 | — |
| Product | 8b-hydroxy-2-(methylamino)-3a,4-dihydroindeno[1,2-d][1,3]thiazole-6-carbonitrile | HCID 178482339 | — |
Reaction Steps
236 mg of 2-bromo-1-oxoindane-5-carbonitrile are dissolved in 10 ml of acetone and, at 0° C., 135 mg of N-methylthiourea are added. The mixture is stirred at room temperature for 3 h and at ice-bath temperature for 90 minutes. The precipitate is filtered off with suction, washed with acetone and dried in vacuo. The hydrobromide of 3a-hydroxy-2-methylamino-8,8a-dihydro-3aH-indeno[1,2-d]thiazole-6-carbonitrile is obtained with a melting point of 287-288° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06235763B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-07d4b75b0cf1426b8076f4cd7b087752 |
| Source note | uspto-grants-2001_05 |