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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743833Generated: October 31, 2026

Sodium cyanoborohydride → HCID 10355071, compound

https://huagongshe.com/reaction/1743833

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 10354976HCID 10354976—
SolventAcetic AcidHCID 176—
ProductHCID 10355071HCID 1035507165%

Reaction Steps

To a solution of 3-methyl-2,3,4,5,9,10,11,12-octahydro-1H-[1,4]diazocino[7,8,1-jk]carbazole (0.46 g, 1.8 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 0.30 g of the title compound as a light oil. 100 mg of this compound was treated with one equivalent of fumaric acid in ethanol to form a fumarate salt, mp 150-153° C. MS (ESI) m/z 257 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07012089B2
Source datasetuspto-grants-2006_03
ORD IDord-e03380182b8a4d08a28efa3eaa57ecf3
Source noteuspto-grants-2006_03