HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 4,10-Dihydro-5H-pyrrolo[1,2-a]thieno[3,2-e][1,4]diazepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | (Dimethyl sulfide)trihydroboron | HCID 12423031 | — |
| Reactant | 5-Oxo-4,5-dihydropyrrolo[1,2-a]thieno[3,2-e][1,4]diazepine | HCID 21837150 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4,10-Dihydro-5H-pyrrolo[1,2-a]thieno[3,2-e][1,4]diazepine | HCID 21836969 | — |
Reaction Steps
To a suspension of 7.0 g of 5-oxo-4,5-dihydro-pyrrolo[1,2-a]thieno[3,2-e][1,4]diazepine in 25 ml of anhydrous tetrahydrofuran is added 9 ml of 10M borane-dimethylsulfide in tetrahydrofuran. The mixture is refluxed for 6 hours. The solution is cooled to room temperature and 25 ml of methanol added dropwise. The volatiles are removed under vacuum. To the residue is added 100 ml of 2N NaOH. The mixture is refluxed 5 hours and filtered. The solid is extracted with dichloromethane and the extract is washed with 2N citric acid, water and dried (Na2SO4). The solvent is removed to give a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05753648 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-30a805942a854c7881551fe675cd3766 |
| Source note | uspto-grants-1998_05 |