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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709298Generated: October 26, 2026

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

https://huagongshe.com/reaction/709298

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactanttert-Butyl (5-methylpyrazin-2-yl)carbamateHCID 22046506—
SolventCarbon TetrachlorideHCID 5943—
Producttert-Butyl (5-(bromomethyl)pyrazin-2-yl)carbamateHCID 4507374075.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution tert-butyl 5-methylpyrazin-2-ylcarbamate (500 mg, 2.39 mmol) in CCl4 (8.0 mL) were added NBS (446 mg, 2.51 mmol) and AIBN (117 mg, 0.72 mmol). The reaction mixture was stirred for 4 hours at 80° C. after which, it was partitioned between CH2Cl2 and water. The organic layer was separated and the aqueous layer was extracted with CH2Cl2. The combined organic extracts were washed with brine, dried over MgSO4, celite filtered and concentrated under reduced pressure. The crude product was purified by flash chromatography using (10% Ethyl acetate/Hexane) as a solvent to afford title compound (520 mg, 75% yield). 1H NMR (600 MHz, CDCl3) δ 9.29 (s, 1H), 8.95 (s, 1H), 8.37 (s, 1H), 4.38 (s, 2H), 1.57 (s, 9H). MS m/z: 288 [M+1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09180127B2
Source datasetuspto-grants-2015_11
ORD IDord-fbcfee93f2a146bd9faeb9b3cf919dd8
Source noteuspto-grants-2015_11