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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811806Generated: November 4, 2026

tert-Butyl piperazine-1-carboxylate → Tert-butyl 4-((6-fluoropyridin-3-yl)methyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1811806

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant5-(Bromomethyl)-2-fluoropyridineHCID 22050638—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 4-((6-fluoropyridin-3-yl)methyl)piperazine-1-carboxylateHCID 5954841484%

Reaction Steps

tert-Butyl piperazine-1-carboxylate (Aldrich, St. Louis, Mo., 17.77 g, 95 mmol) was added to a stirred solution of 5-(bromomethyl)-2-fluoropyridine (15.11 g, 80 mmol) in N,N-dimethylformamide (120 mL) at 0° C. and the suspension was stirred at room temperature overnight. The resulting thick reaction mixture was quenched with cold water (50 mL), the resulting suspension was stirred for 30 min, and the resulting solid was collected and washed with additional cold water (50 mL). The off-white precipitate was dried under vacuum to give the title compound tert-butyl 4-((6-fluoropyridin-3-yl)methyl)piperazine-1-carboxylate (19.7494 g, 66.9 mmol, 84% yield) as a white solid. LCMS (API-ES) m/z 296 (M+H)+; 1H NMR (400 MHz, d6-DMSO) δ 8.13 (s, 1H) 7.90 (td, J=8.02, 1.37 Hz, 1H) 7.15 (dd, J=8.31, 2.05 Hz, 1H) 3.51 (s, 2H) 3.30 (br. s., 4H) 2.10-2.40 (m, 4H) 1.39 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362241B2
Source datasetuspto-grants-2013_01
ORD IDord-c03226f8626c4fb4a7dd5c4e3ef50d9c
Source noteuspto-grants-2013_01