HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 10632014, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 10850843 | HCID 10850843 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 10632014 | HCID 10632014 | 84% |
Reaction Steps
1 g (0.0028 mol) of sodium borohydride is added in small portions to a solution of 2 g (0.007 mol) of 6-piperidino-5,6-dihydro-4-oxo-4H-pyrrolo[1,2-a]thieno -[2,3-f][1,4]diazepine in 120 ml of methanol, and the reaction mixture is stirred at room temperature for 15 minutes and then heated to reflux for 30 minutes. The methanol is then removed under vacuum and the solid residue ground in 200 ml of water. The precipitate is drained, washed with water, dried and recrystallized. 1.2 g of 5,6-dihydro-4-oxo-4H-pyrrolo[1,2-a]-thieno[2,3-f][1,4]diazepine are obtained in the form of white crystals, melting point 191° C. (ethyl ether).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05130301 |
| Source dataset | uspto-grants-1992_07 |
| ORD ID | ord-154e5f38feab4a70918056aafaab89d6 |
| Source note | uspto-grants-1992_07 |