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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743866Generated: November 1, 2026

Sodium cyanoborohydride → HCID 10377267, compound

https://huagongshe.com/reaction/1743866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 10332074HCID 10332074—
SolventAcetic AcidHCID 176—
ProductHCID 10377267HCID 1037726784.6%

Reaction Steps

To a solution of 8-fluoro-2,3,4,5,10,11-hexahydro-1H,9H-cyclopenta[b][1,4]diazocino[7,8,1-hi]indole (0.41 g, 1.68 mmole) in acetic acid (50 mL) was added sodium cyanoborohydride (0.33 g, 4.99 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 0.35 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 169-170° C. MS (ES) m/z 247.13 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07012089B2
Source datasetuspto-grants-2006_03
ORD IDord-045dcdc438c84fecbde3e822a60e08b7
Source noteuspto-grants-2006_03