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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916362Generated: October 27, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → 4-(3-Fluoropiperidin-1-yl)naphthalene-1-carbonitrile

https://huagongshe.com/reaction/916362

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant1-Cyano-4-fluoronaphthaleneHCID 2736734—
Reactant3-FLUOROPIPERIDINE HYDROCHLORIDEHCID 2759156—
SolventSodium HydroxideHCID 14798—
Product4-(3-Fluoropiperidin-1-yl)naphthalene-1-carbonitrileHCID 1157972618.3%

Reaction Conditions

Temperature110 °C

Reaction Steps

3-Fluoropiperidine hydrochloride (106 mg, 0.76 mol) was dissolved in sodium hydroxide (1 M, 10 mL) and extracted with dichloromethane (4×10 mL), the combined extracts were dried over sodium sulfate, filtered and evaporated. Pyridine (2 mL) was added, followed by 1-cyano-4-fluoronaphthalene (108 mg, 0.63 mmol) and the vial was shaken at 110° C. overnight. GC-MS and TLC showed only very little conversion. DBU (10 μL) was added and the shaking was continued for 2 weeks at 110° C., after which GC-MS showed ˜50% conversion. The reaction was worked up in the same way as 165RL60 and purified by silica gel column chromatography eluted with a stepwise gradient of 0-60% ethyl acetate in n-heptane to give the title compound (29.3 mg, 12%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07268232B2
Source datasetuspto-grants-2007_09
ORD IDord-38af6c8514e64e79a72010bed6ca6158
Source noteuspto-grants-2007_09