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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743881Generated: November 2, 2026

Sodium cyanoborohydride → HCID 10422838, compound

https://huagongshe.com/reaction/1743881

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 10244387HCID 10244387—
SolventAcetic AcidHCID 176—
ProductHCID 10422838HCID 1042283849.6%

Reaction Steps

To a solution of 8-chloro-2,3,4,5,10,11-hexahydro-1H,9H-cyclopenta[b][1,4]diazocino[7,8,1-hi]indole (0.60 g, 2.30 mmole) in acetic acid (100 mL) was added sodium cyanoborohydride (0.60 g, 9.07 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% to 5% methanol in methylene chloride) provided 0.30 g of the title compound as a white solid. 60 mg of this compound was further treated with one equivalent of fumaric acid in ethanol to form a fumarate salt, mp 169-170° C. MS (ES) m/z 263.1 ([M+H]+), MS (ES) m/z 304.1 ([M+ACN+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07012089B2
Source datasetuspto-grants-2006_03
ORD IDord-43558da913974df6820c16ca08ab33e4
Source noteuspto-grants-2006_03