Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1,2-Dihydro-6-phenylindolo[1,7-ab][1,5]benzodiazepine | HCID 12519140 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 12519153 | HCID 12519153 | — |
Reaction Steps
A stirred mixture, under N2, of 23.0 g of 1,2-dihydro-6-phenylindolo[1,7-ab][1,5]benzodiazepine in 200 ml of absolute ethanol is cooled to 0°-5° C. Sodium borohydride is then added in small portions and at such a rate as to keep the reaction temperature less than 5° C., and to minimize foaming. About 3 g. are required to discharge the initial blue-purple color, and another 1 g. is added to insure complete reduction. The mixture is then stirred 1 hour at 0° C. and 1 hour at room temperature. Water is added, the product is filtered, washed repeatedly with water, and dried to give 6-phenyl-1,2,6,7-tetrahydroindolo[1,7-ab][1,5]benzodiazepine, m.p. 161°-164° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04186199 |
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| Source dataset | uspto-grants-1980_01 |
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| ORD ID | ord-0a49a73c556843329c3bdcbead38c038 |
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| Source note | uspto-grants-1980_01 |
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