Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Borane | HCID 6331 | — |
| Reactant | HCID 86739322 | HCID 86739322 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86739321 | HCID 86739321 | — |
Reaction Steps
A solution of borane in tetrahydrofuran (1 M, 50 ml) was added carefully to a stirred solution-suspension of 6-chloro-3-cyclohexylcarbonyl-1,2,3,4-tetrahydropyrido[4',3':2,3]indolo[1,7-ab][1,4]benzodiazepin-9(8H)-one (3.0 g) in tetrahydrofuran (100 ml) and the resulting mixture refluxed for 2 hours, cooled and the excess of borane destroyed by dropwise addition of water. The mixture was then evaporated to dryness under reduced pressure and the residue refluxed with a mixture of 1-octene (50 ml) and xylene (80 ml) for 1 hour and xylene and the combined filtrates were evaporated under reduced pressure. The residue was triturated with a small quantity of ether, filtered, and recrystallized from a mixture of 2-propanol and ethanol to yield the title compound, m.p. 230°-233° (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04438120 |
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| Source dataset | uspto-grants-1984_03 |
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| ORD ID | ord-4c5af4b4878f4b6f94aa01cb67a17f76 |
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| Source note | uspto-grants-1984_03 |
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