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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 1-Cyano-4-fluoronaphthalene | HCID 2736734 | — |
| Reactant | 3-FLUOROPIPERIDINE HYDROCHLORIDE | HCID 2759156 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 4-(3-Fluoropiperidin-1-yl)naphthalene-1-carbonitrile | HCID 11579726 | 18.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07268232B2 |
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| Source dataset | uspto-grants-2007_09 |
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| ORD ID | ord-38af6c8514e64e79a72010bed6ca6158 |
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| Source note | uspto-grants-2007_09 |
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