HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 21455225, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N,N-Dimethylaminoethyl chloride hydrochloride | HCID 11636816 | — |
| Reactant | HCID 12521647 | HCID 12521647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21455225 | HCID 21455225 | — |
Reaction Steps
A mixture of 0.31 g. of 55% sodium hydride-mineral oil dispersion and 0.50 g. of dimethylaminoethylchloride hydrochloride in 25 ml. of dry dimethylformamide is stirred at room temperature for 0.5 hours. To the mixture is added 0.43 g. of 4,9-dihydro-4-ethyl-10H-thieno[3,4-b] [1,5]benzodiazepin-10-one and stirring is continued for 18 hours. The reaction mixture is cooled, quenched with water, and extracted with chloroform. The dried chloroform extracts are concentrated to an oil, which is purified by preparative thin layer chromatography on silica gel with 10:1 benzene-methanol as eluent. The oily solid thus obtained is recrystallized from hexane to give white crystals, m.p. 75°-77°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03953430 |
| Source dataset | uspto-grants-1976_04 |
| ORD ID | ord-0e9d03a370a3472ea387556c0d582fe8 |
| Source note | uspto-grants-1976_04 |