HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1407112Generated: October 30, 2026
Methanamine, N-methoxy-, hydrochloride (1:1) → HCID 59436218, compound
https://huagongshe.com/reaction/1407112
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | HCID 59436290 | HCID 59436290 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59436218 | HCID 59436218 | 60% |
Reaction Steps
To a solution of N,O-dimethylhydroxylamine hydrochloride (2.63 g, 27 mmol) and iPr2NEt (4.70 mL, 27 mmol) in CH2Cl2 (30 mL) was added AlMe3 (1.8 M solution in toluene, 15 mL, 27 mmol) dropwise at 0° C. under Ar atmosphere. After stirring for 1 h, a solution of methyl 5-(methoxymethyl)-4-oxo-1-[3-(trifluoromethyl)phenyl]-1,4-dihydropyridazine-3-carboxylate (3.08 g, 9 mmol) in CH2Cl2 (30 mL) was added dropwise, and the mixture was stirred for 1 h at 0° C. The reaction mixture was poured into ice-water and extracted with AcOEt. The extract was washed with brine, dried over MgSO4, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography eluting with AcOEt and recrystallized from hexane/AcOEt to give the title compound (1.99 g, 60% yield) as an off-white solid: mp 157-159° C.; 1H NMR (300 MHz, CDCl3): δ ppm 3.41 (3H, s), 3.53 (3H, s), 3.67 (3H, s), 4.50 (2H, d, J=1.1 Hz), 7.62-7.71 (2H, m), 7.79-7.85 (1H, m), 7.90 (1H, s), 8.39 (1H, t, J=1.1 Hz). Anal. Calcd for C16H16F3N3O4: C, 51.75; H, 4.34; N, 11.32. Found: C, 51.77; H, 4.25; N, 11.24.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08916566B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-11237d2e09a54ccb9ea77a8b7f9a6df3 |
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| Source note | uspto-grants-2014_12 |
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