HuagongsheHuagongshe Chemistry Print Report · For research reference only
Semicarbazide → Aminobenzophenone semicarbazone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Semicarbazide | HCID 5196 | — |
| Reactant | 2-Aminobenzophenone | HCID 76080 | — |
| Product | Aminobenzophenone semicarbazone | HCID 620280 | — |
Reaction Steps
A number of methods for preparing 1,3,4-benzotriazepine-2-ones have been described in the literature. In general, the compounds are prepared by either of two methods from a 2-aminobenzophenone. In the first method, the 2-aminobenzophenone is treated with semicarbazide to give an aminobenzophenone semicarbazone. This product is cyclized to give the benzotriazepine-2-one. See Bull. Chem. Soc. Jap., 43, 135-138 (1970); Japanese publications 70 11,148 (CA 73:25544a) and 70 11,147 (CA 73:25545b). Alternately, a 2-amino-benzophenone hydrazone is treated with phosgene to give the desired benzotriazepine-2-one. See U.S. Pat. No. 3,176,008; J. Pharm. Sci. 63 (b), 838-41 (1974) and J. Med. Chem. 7(3), 386 (1964).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04144233 |
| Source dataset | uspto-grants-1979_03 |
| ORD ID | ord-effc535b2291428fb6cc2d67d24afefc |
| Source note | uspto-grants-1979_03 |