HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 5,6,7,8-Tetrahydro-2-phenyl-3-(benzoylaminoiminomethyl)imidazo[2,1-b]benzothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Benzoylhydrazine | HCID 11955 | — |
| Reactant | 2-Phenyl-4,5,6,7,8-pentahydroimidazo[2,1-b]benzothiazole-3-carbaldehyde | HCID 10731614 | — |
| Reactant | Ethanol hydrochloride | HCID 21887872 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5,6,7,8-Tetrahydro-2-phenyl-3-(benzoylaminoiminomethyl)imidazo[2,1-b]benzothiazole | HCID 2314510 | 84% |
Reaction Steps
0.28 g of 5,6,7,8-tetrahydro-2-phenyl-3-formylimidazo[2,1-b]benzothiazole and 0.15 g of benzohydrazide were stirred over night in 20 ml of a 0.1N hydrochloric acid-ethanol solution at room temperature and the precipitated crystal obtained by filtration. The crystals were dissolved in water and the solution was made alkaline by ammonia solution, then extracted by chloroform. The extract was washed with water and dried, then the solvent was distilled off and the residue was crystallized from ethyl acetate to obtain the desired substance in an amount of 0.35 g (yield of 84.0%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05919799 |
| Source dataset | uspto-grants-1999_07 |
| ORD ID | ord-6b09b8036967419295bf960b4f73ea62 |
| Source note | uspto-grants-1999_07 |