HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 178502646, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 73165016 | HCID 73165016 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178502646 | HCID 178502646 | — |
Reaction Steps
A mixture of 0.5 g of 7-chloro-5-(2-fluorophenyl)-N-methoxy-α-nitro-3H-1,4-benzodiazepine-2-methanimine 4-oxide, 10 ml of ethanol, 5 ml of tetrahydrofuran and 0.4 g of sodium borohydride was stirred at ambient temperature for 1 hr. After partitioning between methylene chloride and aqueous sodium bicarbonate solution, the organic phase was dried and evaporated. Chromatography of the residue over 7 g of silica gel yielded 7-chloro-5-(2-fluorophenyl)-2,3-dihydro-N-methoxy-1H-1,4-benzodiazepine-2-methanimine 4-oxide as light yellow resin.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04226771 |
| Source dataset | uspto-grants-1980_10 |
| ORD ID | ord-2c9ca2f4dd4f418a863978b26a4cd442 |
| Source note | uspto-grants-1980_10 |