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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743846Generated: October 31, 2026

Sodium cyanoborohydride → HCID 10468723, compound

https://huagongshe.com/reaction/1743846

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 10061933HCID 10061933—
SolventAcetic AcidHCID 176—
ProductHCID 10468723HCID 1046872332.7%

Reaction Steps

To a solution of 6-chloro-3-methyl-2,3,4,5,10,11-hexahydro-1H,9H-cyclopenta[b][1,4]diazocino[7,8,1-hi]indole (0.20 g, 0.73 mmole) in acetic acid (50 mL) was added excess sodium cyanoborohydride (0.23 g, 3.65 mmole) and the reaction mixture was stirred at room temperature for 5 hours. The solvent was removed in vacuo and the residue was diluted with ethyl acetate (200 mL) and washed with saturated sodium bicarbonate (150 mL), saturated sodium chloride (150 mL), dried (sodium sulfate) and concentrated. Purification by flash column chromatography (silica gel, ethyl acetate:hexanes 3:2) provided 66 mg of the title compound. This was further treated with one equivalent of fumaric acid in ethanol to form a fumarate salt, mp 196-9° C. MS (ESI) m/z 277 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07012089B2
Source datasetuspto-grants-2006_03
ORD IDord-50c3a39a8e154bf8968efef92326e829
Source noteuspto-grants-2006_03