HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743834Generated: November 1, 2026
Sodium cyanoborohydride → HCID 10466921, compound
https://huagongshe.com/reaction/1743834
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 10354280 | HCID 10354280 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 10466921 | HCID 10466921 | 61.9% |
Reaction Steps
To a solution 2,3,4,5,9,10,11,12-octahydro-1H-[1,4]diazocino[7,8,1-jk]carbazole (0.20 g, 0.80 mmole) in acetic acid (50 mL) was added sodium cyanoborohydride (0.30 g, 4.5 mmol) and the reaction mixture was stirred at room temperature for 1 hour. The solvent was removed in vacuo and the residue was diluted with ethyl acetate (300 mL) and washed with saturated aqueous sodium bicarbonate (150 mL) and saturated aqueous sodium chloride (150 mL), dried (sodium sulfate) and concentrated in vacuo. Purification by flash column chromatography (silica gel, ethyl acetate:hexanes 3:2) provided 0.12 g of the title compound as an oil. This compound was treated with one equivalent of fumaric acid in ethanol to form a fumarate salt, mp 169-171° C. MS (ESI) m/z 243 ([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-69b598f0e18b4dcabebec904929852a2 |
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| Source note | uspto-grants-2006_03 |
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