HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 9-[4-chloro-3-(trifluoromethyl)benzyl]-4,9-dihydro-10H-thieno[3,4-b][1,5]benzodiazepin-10-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4,9-dihydro-10H-thieno[3,4-b][1,5]benzodiazepin-10-one | HCID 12521641 | — |
| Reactant | 1-Chloro-4-(chloromethyl)-2-(trifluoromethyl)benzene | HCID 13094262 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 9-[4-chloro-3-(trifluoromethyl)benzyl]-4,9-dihydro-10H-thieno[3,4-b][1,5]benzodiazepin-10-one | HCID 20392258 | — |
Reaction Steps
To a solution of 8.64 g. of 4,9-dihydro-10H-thieno[3,4-b][1,5]benzodiazepin-10-one in 100 ml. of dimethylformamide is added 2.1 g. of 50% sodium hydride in mineral oil. The mixture is stirred for one hour and 10.0 g. of 4-chloro-3-trifluoromethyl benzyl chloride and 10 mg of potassium iodide are added. The mixture is stirred for a prolonged period and the solvent is removed in vacuo. The residual gum is dissolved in methylene chloride, dried over magnesium sulfate and filtered through magnesol. The filtrate is evaporated to give tan crystals which are recrystallized from ethanol giving the desired product as off-white crystals, mp. 181°-183° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04168269 |
| Source dataset | uspto-grants-1979_09 |
| ORD ID | ord-4b9804bd98b641c691ff56b341ba740a |
| Source note | uspto-grants-1979_09 |