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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743867Generated: October 31, 2026

Sodium cyanoborohydride → HCID 10244368, compound

https://huagongshe.com/reaction/1743867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 10220778HCID 10220778—
SolventAcetic AcidHCID 176—
ProductHCID 10244368HCID 1024436876.2%

Reaction Steps

To a solution of 8-fluoro-2,3,4,5,9,10,11,12-octahydro-1H-[1,4]diazocino[7,8,1-jk]carbazole (0.30 g, 1.16 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 for 4 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 0.23 g 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 189-190° C. MS (ESI) m/z 261 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07012089B2
Source datasetuspto-grants-2006_03
ORD IDord-c158754a7ed64f809ac4f4f35ac99953
Source noteuspto-grants-2006_03