HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596081Generated: November 2, 2026
N-bromobutanimide → Methyl 4-(2-amino-5-bromopyridin-3-yl)-2-methylbenzoate
https://huagongshe.com/reaction/596081
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Methyl 4-(2-aminopyridin-3-yl)-2-methylbenzoate | HCID 118046459 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 4-(2-amino-5-bromopyridin-3-yl)-2-methylbenzoate | HCID 118045889 | — |
Reaction Steps
To a solution of methyl 4-(2-aminopyridin-3-yl)-2-methylbenzoate (4.2 g, 17.34 mmol) in acetonitrile (173 mL) was added NBS (3.15 g, 17.68 mmol) in two portions at 0° C. The reaction mixture was stirred at 0° C. for 20 min. LCMS showed the reaction completed. After quenched with sat. Na2SO3 and NaHCO3, the reaction mixture was stirred for 30 min. The reaction mixture was extracted with EtOAc 3 times, washed by sat NaHCO3, water and brine. The organics was dried over Na2SO4, filtered and concentrated. The crude material was triturated with ether and taken to the next step without further purification. LCMS (m/z): 323.1 (MH+), 0.68 min.
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-4829d1540229494ab22631d82ec9770f |
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| Source note | uspto-grants-2016_01 |
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