HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743881Generated: November 2, 2026
Sodium cyanoborohydride → HCID 10422838, compound
https://huagongshe.com/reaction/1743881
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 10244387 | HCID 10244387 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 10422838 | HCID 10422838 | 49.6% |
Reaction Steps
To a solution of 8-chloro-2,3,4,5,10,11-hexahydro-1H,9H-cyclopenta[b][1,4]diazocino[7,8,1-hi]indole (0.60 g, 2.30 mmole) in acetic acid (100 mL) was added sodium cyanoborohydride (0.60 g, 9.07 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 0.30 g of the title compound as a white solid. 60 mg of this compound was further treated with one equivalent of fumaric acid in ethanol to form a fumarate salt, mp 169-170° C. MS (ES) m/z 263.1 ([M+H]+), MS (ES) m/z 304.1 ([M+ACN+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-43558da913974df6820c16ca08ab33e4 |
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| Source note | uspto-grants-2006_03 |
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