HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497227Generated: October 26, 2026
Triethylamine → 2-Amino-3-fluoro-N-methoxy-N-methyl-benzamide
https://huagongshe.com/reaction/1497227
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Reactant | 8-Fluoroisatoic anhydride | HCID 10535393 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Amino-3-fluoro-N-methoxy-N-methyl-benzamide | HCID 81507492 | 80.4% |
Reaction Steps
To a suspension of N,O-dimethylhydroxylamine hydrochloride (703 mg, 7.21 mmol) in ethanol (5.4 ml) and water (0.6 ml) was added triethylamine (729 mg, 1.00 ml, 7.21 mmol) and the mixture was stirred for 10 min at room temperature. Then 8-fluoro-1H-benzo[d][1,3]oxazine-2,4-dione (870 mg, 4.8 mmol) and additional ethanol (2 ml) were added and the reaction mixture was heated to reflux for 3.5 h. After cooling to room temperature, the mixture was poured onto ice/saturated NaHCO3-solution, extracted with EtOAc and the combined extracts were washed with water and brine, dried with Na2SO4 and evaporated. The remaining residue was purified by column chromatography (silica gel, heptane/EtOAc 80:20-70:30) to afford the title compound (765 mg, 80%) as light brown oil. MS (ESI): 199.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09199938B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-257c720c80f5445db144cbd6c40acd8b |
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| Source note | uspto-grants-2015_12 |
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