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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1169824Generated: October 27, 2026

2-Fluoropyridine → Tert-butyl 4-cyano-4-(pyridin-2-YL)piperidine-1-carboxylate

https://huagongshe.com/reaction/1169824

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-FluoropyridineHCID 9746—
ReactantTert-butyl 4-cyanopiperidine-1-carboxylateHCID 1514443—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
SolventTolueneHCID 1140—
SolventSodium chloride; waterHCID 57417360—
ProductTert-butyl 4-cyano-4-(pyridin-2-YL)piperidine-1-carboxylateHCID 53439111—

Reaction Steps

To a solution of 2-fluoro-pyridine (5.83 g, 60 mmole) in toluene (40 mL) was added tert-butyl 4-cyanopiperidine-1-carboxylate (I-1) (4.22 g, 20 mmole) and 0.5M solution of KHMDS (48 mL, 24 mmole). The reaction mixture was stirred 2 h at rt ° C. After this time, LCMS indicated that the reaction was completion. The reaction mixture was poured into brine (150 mL) and extracted with EtOAc (3×150 mL). The combined organic extracts were washed with brine (2×100 mL), dried over MgSO4, filtered and concentrated to afford the desired product tert-butyl 4-cyano4-pyridin-2-ylpiperidine-1-carboxylate (I-2) as a yellow-brown solid. Analytical LCMS: single peak (214 mm), 3.076 min. This product was used in next step reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07825135B2
Source datasetuspto-grants-2010_11
ORD IDord-060b496a48b74d938558cfeddc99d528
Source noteuspto-grants-2010_11