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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743878Generated: November 1, 2026

Sodium cyanoborohydride → HCID 10017135, compound

https://huagongshe.com/reaction/1743878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 10356798HCID 10356798—
SolventAcetic AcidHCID 176—
ProductHCID 10017135HCID 1001713532%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07012089B2
Source datasetuspto-grants-2006_03
ORD IDord-34af895d358c4fde84cebdaab65c8234
Source noteuspto-grants-2006_03