HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 4,9-Dihydro-9-(2-dimethylaminoathyl)-4-methyl-thieno[3,4-b][1,5]benzodiazepin-10-on
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N,N-Dimethylaminoethyl chloride hydrochloride | HCID 11636816 | — |
| Reactant | 4,9-Dihydro-4-methyl-10H-thieno[3,4-b][1,5]benzodiazepin-10-one | HCID 12521642 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4,9-Dihydro-9-(2-dimethylaminoathyl)-4-methyl-thieno[3,4-b][1,5]benzodiazepin-10-on | HCID 21455235 | — |
Reaction Steps
A mixture of 0.4 g. of 55% sodium hydride-mineral oil dispersion 0.5 g. of 2-dimethylaminoethylchloride hydrochloride and 25 ml. of dry dimethylformamide is stirred at room temperature for 0.5 hours. To the mixture is added 0.4 g. of 4,9-dihydro-4-methyl-10H-thieno[3,4-b][1,5]benzodiazepin-10-one and stirring at room temperature is continued for 18 hours. The reaction mixture is cooled, quenched with water, acidified, decolorized and filtered. The filtrate is made alkaline and extracted with chloroform. The dried chloroform extracts are concentrated to give a solid which is recrystallized from chloroform-hexane to give off-white crystals, m.p. 147°-149° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04007272 |
| Source dataset | uspto-grants-1977_02 |
| ORD ID | ord-c9e7d6ef85e841e3adf6f9cc812d07ff |
| Source note | uspto-grants-1977_02 |