Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 9970596 | HCID 9970596 | — |
| Product | HCID 10470332 | HCID 10470332 | — |
Reaction Steps
To a solution of 6-chloro-2,3,4,5,9,10,11,12-octahydro-1H-[1,4]diazocino[7,8,1-jk]carbazole (0.20 g, 0.73 mmole) in acetic acid (50 mL) was added excess sodium cyanoborohydride (0.23 g, 3.65 mmole) and the reaction mixture was stirred at room temperature overnight. The solvent was removed in vacuo and the residue was diluted with methylene chloride (200 mL) and washed with aqueous sodium hydroxide (1N, 150 mL), saturated sodium chloride (150 mL), dried (sodium sulfate) and concentrated. Purification by flash column chromatography (silica gel, 1.5% to 5% methanol in methylene chloride) provided 0.10 g of the title compound. This compound was treated with one equivalent of fumaric acid in ethanol to form a fumarate salt, mp 184-187° C. MS (ESI) m/z 305 ([M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07012089B2 |
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| Source dataset | uspto-grants-2006_03 |
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| ORD ID | ord-3fa5cd4ee06e4687b82a35062a5e24d5 |
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| Source note | uspto-grants-2006_03 |
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