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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749372Generated: October 30, 2026

Sodium hydride → HCID 86681867, compound

https://huagongshe.com/reaction/1749372

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-Cyano-2-fluoropyridineHCID 12002587—
Reactant2490154-94-2HCID 86681866—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 86681867HCID 86681867—

Reaction Steps

A solution of tert-butyl (2R,5R)-5-hydroxy-2-methylpiperidine-1-carboxylate (4.50 g, 22.9 mmol) in DMSO (42 mL) was treated with NaH (0.60 g, 25.1 mmol) in portions, then allowed to stir for 15 min. Solid 4-cyano-2-fluoropyridine (3.83 g, 31.4 mmol) was then added and the reaction was stirred at RT overnight. The reaction was quenched by addition of saturated, aqueous NaHCO3, then diluted further with water. The mixture was extracted three times with EtOAc. The organics were washed with brine, dried over MgSO4, filtered, and concentrated. The crude material was purified by silica gel gradient chromatography (0-25% ethyl acetate in hexanes), providing the titled compound as a colorless oil which quickly solidified to give white crystals. 1H NMR (400 MHz, CDCl3) δ 8.27 (d, J=5.2 Hz, 1H), 7.05 (dd, J=5.18, 1.3 Hz, 1H), 6.96 (d, J=1.1 Hz, 1H), 5.16 (s, 1H), 4.51 (s, 1H), 4.34 (d, J=15.0 Hz, 1H), 3.05-3.08 (m, 2H), 2.07-2.20 (m, 1H), 1.89-1.95 (m, 2H), 1.35-1.38 (m, 2H), 1.30 (s, 9H), 1.19 (d, J=7.2 Hz, 3H) ppm. LRMS m/z (M+H) 318.4 found, 318.2 required.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156819B2
Source datasetuspto-grants-2015_10
ORD IDord-5570b880b39743c18dc43b2b7a8a250f
Source noteuspto-grants-2015_10