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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743851Generated: November 2, 2026

Sodium cyanoborohydride → HCID 10062837, compound

https://huagongshe.com/reaction/1743851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 10446856HCID 10446856—
SolventAcetic AcidHCID 176—
ProductHCID 10062837HCID 1006283733.4%

Reaction Steps

To a solution of 6-chloro-2,3,4,5,10,11,12,13-octahydro-1H,9H-cyclohepta[b][1,4]diazocino[7,8,1-hi]indole (0.20 g, 0.69 mmole) in acetic acid (50 mL) was added excess sodium cyanoborohydride (0.21 g, 3.45 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 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 67 mg of the title compound. This compound was treated with one equivalent of fumaric acid in ethanol to form a fumarate salt, mp 168-170° 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-36adca6bc76a43aabbb2ed178f3a9f32
Source noteuspto-grants-2006_03