HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 11H-imidazo[1,2-c][1,3]benzodiazepine-5(6H)-thione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thiophosgene | HCID 10040 | — |
| Reactant | 2-[(1H-Imidazol-2-yl)methyl]aniline | HCID 13344903 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 11H-imidazo[1,2-c][1,3]benzodiazepine-5(6H)-thione | HCID 13344904 | — |
Reaction Steps
Dichloromethane (42,000 ml) and 5,120 g (50.65 moles) of triethylamine are charged into a 20 gallon flask. The solution is stirred under nitrogen atmosphere and 4,370 g (25.23 moles) of 2-(2-aminobenzyl)imidazole were added. The suspension is cooled to 0°-5° and 3,421 g (29.75 moles) of 85% thiophosgene in carbon tetrachloride are added over 3 hours, during which time the reaction temperature rises slowly to 15°. The suspension is then stirred at 10° for 4 hours and at ambient temperature overnight. The precipitated product is collected, washed with 2×3000 ml of dichloromethane and 5×4000 ml of water, and dried (5 mm Hg/60°) to give 11H-imidazo[1,2-c][1,3]benzodiazepine-5(6H)-thione, m.p. 182°-183°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04507311 |
| Source dataset | uspto-grants-1985_03 |
| ORD ID | ord-db16f53a5ddb4f8c93b2092248623d9e |
| Source note | uspto-grants-1985_03 |