HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420519Generated: October 30, 2026
N-bromobutanimide → Methyl 2-amino-5-bromoisonicotinate
https://huagongshe.com/reaction/420519
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Methyl 2-aminopyridine-4-carboxylate | HCID 236984 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 2-amino-5-bromoisonicotinate | HCID 25307230 | 35.4% |
Reaction Steps
A solution of 2-amino-isonicotinic acid methyl ester (5.58 g, 36.7 mmol) in DMF (56 mL) was cooled to −18° C. (ice/MeOH bath), treated with NBS (7.21 g, 38.5 mmol), and stirred at −18° C. for 1 h. The reaction mixture was diluted in AcOEt (500 mL) and washed with water (2×250 mL). The organic layer was dried over Na2SO4, filtered and evaporated to yield the crude title compound (3.0 g, 13.0 mmol, 35%) as a yellow solid, which was used in the next step without further purification. MS: 231 [M+1]+; HPLC: AtRet=0.70.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08097617B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-e9ee3d3716b4441ea531b3b4e400860c |
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| Source note | uspto-grants-2012_01 |
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