HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743878Generated: November 1, 2026
Sodium cyanoborohydride → HCID 10017135, compound
https://huagongshe.com/reaction/1743878
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 10356798 | HCID 10356798 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 10017135 | HCID 10017135 | 32% |
Reaction Steps
To a solution of 8-chloro-3-methyl-2,3,4,5,9,10,11,12-octahydro-1H-[1,4]diazocino[7,8,1-jk]carbazole (0.25 g, 0.86 mmole) in acetic acid (50 mL) was added sodium cyanoborohydride (0.22 g, 3.32 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% methanol in methylene chloride) provided 80 mg of the title compound as a colorless oil. The oil was further treated with one equivalent of fumaric acid in ethanol to form a fumarate salt, mp 178-180° C. MS (ESI) m/z 291 ([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-34af895d358c4fde84cebdaab65c8234 |
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| Source note | uspto-grants-2006_03 |
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