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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| 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 | 75.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09180127B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-fbcfee93f2a146bd9faeb9b3cf919dd8 |
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| Source note | uspto-grants-2015_11 |
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