HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109312Generated: November 1, 2026
Methyl 3-amino-4-methylbenzoate → HCID 58861443, compound
https://huagongshe.com/reaction/2109312
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl 3-amino-4-methylbenzoate | HCID 337778 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-(2-Bromoacetyl)pyridine hydrobromide | HCID 2776234 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 58861443 | HCID 58861443 | 16.7% |
Reaction Steps
To a solution of 2-bromo-1-pyridin-3-yl-ethanone hydrobromide (Barlin, G. B. et al. Australian J. Chem, 1989, 1735) (500 mg, 1.78 mmol) in 2 ml of EtOH was added 3-amino-4-methyl-benzoic acid methyl ester (Lancaster; 294 mg, 1.78 mmol) and NaHCO3 (750 mg, 8.9 mmol), and the mixture was stirred for 2 h. The mixture was then filtered and washded with MeOH, then the filtrated was concentrated to a small volume and dissolved in EtOAc. The EtOAc slurry was washed with water and brine, and the washes were extracted once more with EtOAc. The combined organic portions were dried with Na2SO4, filtered, concentrated, and chromatographed (0-5% MeOH in dichloromethane) to provide 84.5 mg of 4-methyl-3-(2-oxo-2-pyridin-3-yl-ethylamino)-benzoic acid methyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07514458B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-9b7b08664e184237b3e77bbe88d39cdb |
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| Source note | uspto-grants-2009_04 |
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