HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 12521646, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | HCID 20355327 | HCID 20355327 | — |
| Reactant | HCID 20355348 | HCID 20355348 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12521646 | HCID 12521646 | — |
Reaction Steps
To a suspension of 0.53 g. of the mixture of 7-chloro-4-methyl-1,3,4,9-tetrahydro-10H-thieno[3,4-b][1,5]benzodiazepin-10-one and 6-chloro-9-methyl-1,3,4,9-tetrahydro-10H-thieno[3,4-b][1,5]benzodiazepin-10-one (prepared as described in Example 17) in 5 ml. of dry pyridine is added, in portions, 0.27 g. of N-chlorosuccinimide. The resulting solution is heated on a steam bath for 15-20 minutes, cooled, diluted with water and filtered. The solid is recrystallized from methanol to give a yellow solid which consists of the single isomer of the title, m.p. 244°-246° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04087421 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-b3fb5c221f92411caf493762d122cf9c |
| Source note | uspto-grants-1978_05 |