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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595901Generated: October 26, 2026

N-bromobutanimide → tert-Butyl (5-(bromomethyl)pyrazin-2-yl)carbamate

https://huagongshe.com/reaction/595901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactanttert-Butyl (5-methylpyrazin-2-yl)carbamateHCID 22046506—
SolventCarbon TetrachlorideHCID 5943—
Producttert-Butyl (5-(bromomethyl)pyrazin-2-yl)carbamateHCID 45073740—

Reaction Conditions

Temperature85 °C

Reaction Steps

A solution of tert-butyl 5-methylpyrazin-2-ylcarbamate (2.79 g, 13.33 mmol), NBS (2.61 g, 14.67 mmol) and AlBN (0.219 g, 1.33 mmol) in CCl4 (45 mL) was purged with Argon, then the solution was heated with 85° C. oil bath for 4 h. The reaction mixture was cooled to room temperature, concentrated and the residue was redissolved in EtOAc (˜50 mL), washed with dilute aqueous NaOH twice (10 mL 1 N NaOH diluted in 20 mL H2O), brine (30 mL), dried (Na2SO4) and concentrated. The residue was further purified by flash chromatography on silica gel eluted with gradient EtOAc/CH2Cl2 (0-30%) and tert-butyl 5-(bromomethyl)pyrazin-2-ylcarbamate was obtained in off-white solid. LCMS (m/z): 288.1/290.1 (MH+), 0.82 min; 1H NMR (400 MHz, CDCl3) δ ppm 9.26 (s, 1H), 8.32 (d, J=1.2 Hz, 1H), 7.62 (br. s., 1H), 4.56 (s, 2H), 1.56 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242996B2
Source datasetuspto-grants-2016_01
ORD IDord-4443b3e244824b1f9506d440f4c513ac
Source noteuspto-grants-2016_01