HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170306Generated: October 26, 2026
Methanamine, N-methoxy-, hydrochloride (1:1) → 6-acetamido-3-bromo-N-methoxy-N-methylpicolinamide
https://huagongshe.com/reaction/2170306
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | 3-Bromo-6-acetamidopyridine-2-carboxylic acid | HCID 25306988 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-acetamido-3-bromo-N-methoxy-N-methylpicolinamide | HCID 90280477 | — |
Reaction Steps
HATU (1-[Bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium 3-oxid hexafluorophosphate) (4.56 g, 12.0 mmol) was added to a solution of 6-acetamido-3-bromopicolinic acid (2.6 g, 10.0 mmol) and DIPEA (N,N-diisopropylethylamine)(5.2 ml, 30 mmol) in DCM (dichloromethane)(10 ml). After 10 minutes, N,O-dimethylhydroxylamine hydrochloride (1.5 g, 15.0 mmol) was added to the reaction. The reaction was stirred at room temperature for 5 min. The reaction mixture was partitioned between EtOAc (ethyl acetate) and saturated NH4Cl solution. The organic phase was washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. The crude material was used in the next step without further purification. MS (m/z) 302.1 [M+H]+. 1H NMR (400 MHz, cd3cl) δ 8.14 (s, 1H), 8.13 (d, J=8.4 Hz, 1H), 7.85 (d, J=8.4 Hz, 1H), 3.56 (s, 3H), 3.37 (s, 3H), 2.20 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09050344B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-09ae41a2569b4559a9b8ed40f4786d39 |
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| Source note | uspto-grants-2015_06 |
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