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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743862Generated: November 1, 2026

Sodium cyanoborohydride → HCID 10445330, compound

https://huagongshe.com/reaction/1743862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 10422650HCID 10422650—
SolventAcetic AcidHCID 176—
ProductHCID 10445330HCID 1044533047.5%

Reaction Steps

To a solution of 8-fluoro-3-methyl-2,3,4,5,10,11-hexahydro-1H,9H-cyclopenta[b][1,4]diazocino[7,8,1-hi]indole (0.23 g, 0.89 mmole) in acetic acid (50 mL) was added sodium cyanoborohydride (95 wt. %, 0.20 g, 3.02 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 0.11 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 180-182° C. MS (ES) m/z 261.13 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07012089B2
Source datasetuspto-grants-2006_03
ORD IDord-12bd53da569543c6a8c68fa5f4dc0c49
Source noteuspto-grants-2006_03