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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581695Generated: November 1, 2026

8-Methoxy-2,3,4,5,6,7-hexahydroazocine → 3-(1-Phenylcyclohexyl)-5,6,7,8,9,10-hexahydro[1,2,4]triazolo[4,3-a]azocine

https://huagongshe.com/reaction/1581695

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-Methoxy-2,3,4,5,6,7-hexahydroazocineHCID 12261059—
Reactant1-(4-Chlorophenyl)cyclohexanecarbohydrazideHCID 22722146—
SolventTolueneHCID 1140—
Product3-(1-Phenylcyclohexyl)-5,6,7,8,9,10-hexahydro[1,2,4]triazolo[4,3-a]azocineHCID 10403095—

Reaction Conditions

Temperature120 °C

Reaction Steps

Anhydrous toluene was added to a mixture of 1-(4-chlorophenyl)cyclohexanecarbohydrazide (62 mg) and 8-methoxy-2,3,4,5,6,7-hexahydroazocine (40.1 mg). The reaction vessel was heated to 120° C. overnight, whereupon it was cooled to room temperature and the solvent was evaporated. The crude product was purified by column chromatography to give 3-(1-phenylcyclohexyl)-5,6,7,8,9,10-hexahydro[1,2,4]triazolo[4,3-α]azocine (2-51) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06730690B2
Source datasetuspto-grants-2004_05
ORD IDord-74cc00131cc548ffb375dccc7107238e
Source noteuspto-grants-2004_05