HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 4,9-Dihydro-4-methyl-10H-thieno[3,4-b][1,5]benzodiazepin-10-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | 1,3,4,9-tetrahydro-4-methyl-10H-thieno[3,4-b] [1,5]benzodiazepin-10-one | HCID 12521632 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4,9-Dihydro-4-methyl-10H-thieno[3,4-b][1,5]benzodiazepin-10-one | HCID 12521642 | — |
Reaction Steps
To a suspension of 3.8 g. of 1,3,4,9-tetrahydro-4-methyl-10H-thieno[3,4-b][1,5]benzodiazepin-10-one in 15 ml. of dry pyridine is added, in portions, a total of 2.18 g. of N-chlorosuccinimide. The resulting solution is heated on a steam bath for 15 minutes, cooled and diluted with water. The solid is collected and recrystallized from methanol, to give a tan solid, m.p. 224°-225° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04007272 |
| Source dataset | uspto-grants-1977_02 |
| ORD ID | ord-0d787f726bd144aca98702dae85e0727 |
| Source note | uspto-grants-1977_02 |