HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743851Generated: November 2, 2026
Sodium cyanoborohydride → HCID 10062837, compound
https://huagongshe.com/reaction/1743851
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 10446856 | HCID 10446856 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 10062837 | HCID 10062837 | 33.4% |
Reaction Steps
To a solution of 6-chloro-2,3,4,5,10,11,12,13-octahydro-1H,9H-cyclohepta[b][1,4]diazocino[7,8,1-hi]indole (0.20 g, 0.69 mmole) in acetic acid (50 mL) was added excess sodium cyanoborohydride (0.21 g, 3.45 mmole) and the reaction mixture was stirred at room temperature for 5 hours. 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 67 mg of the title compound. This compound was treated with one equivalent of fumaric acid in ethanol to form a fumarate salt, mp 168-170° 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-36adca6bc76a43aabbb2ed178f3a9f32 |
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| Source note | uspto-grants-2006_03 |
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