HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorosuccinimide → HCID 20515893, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | HCID 20515888 | HCID 20515888 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 20515893 | HCID 20515893 | — |
Reaction Steps
0.56 g (2.6 mmol) of 4,5-dihydro-5-methyl-6H-imidazo[1,5-a]pyrido[2,3-f][1,4]diazepin-6-one and 0.35 g (2.6 mmol) of N-chlorosuccinimide are treated with 10 ml of dimethylformamide and the mixture is stirred at 90°-100° for 30 minutes. After evaporation to dryness, the residue is chromatographed on silica gel using chloroform containing 4% methanol for the elution. After recrystallization from ethyl acetate, there is obtained 3-chloro-4,5-dihydro-5-methyl-6H-imidazo[1,5-a]pyrido[2,3-f][1,4]diazepin-6-one of melting point 247°-248°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04362732 |
| Source dataset | uspto-grants-1982_12 |
| ORD ID | ord-4b11f690e9e948e59193271d1c1b1eb8 |
| Source note | uspto-grants-1982_12 |