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
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | tert-Butyl (5-methylpyrazin-2-yl)carbamate | HCID 22046506 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | tert-Butyl (5-(bromomethyl)pyrazin-2-yl)carbamate | HCID 45073740 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242996B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-4443b3e244824b1f9506d440f4c513ac |
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| Source note | uspto-grants-2016_01 |
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