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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895113Generated: October 28, 2026

Methanamine, N-methoxy-, hydrochloride (1:1) → HCID 86643930, compound

https://huagongshe.com/reaction/1895113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
ReactantDiisopropylethylamineHCID 81531—
ReactantTrimethylaluminumHCID 16682925—
ReactantMethyl 5-methoxy-4-oxo-1-[3-(trifluoromethyl)phenyl]-1,4-dihydropyridazine-3-carboxylateHCID 59436268—
SolventDichloromethaneHCID 6344—
ProductHCID 86643930HCID 8664393067%

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-methoxy-4-oxo-1-[3-(trifluoromethyl)phenyl]-1,4-dihydropyridazine-3-carboxylate (2.95 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 basic silica gel column chromatography eluting with AcOEt and recrystallized from hexane/AcOEt to give the title compound (2.15 g, 67% yield) as off-white crystals: mp 170-171° C.; 1H NMR (300 MHz, CDCl3): δ ppm 3.41 (3H, s), 3.71 (3H, s), 3.98 (3H, s), 7.63-7.71 (2H, m), 7.80-7.86 (1H, m), 7.88 (1H, s), 7.98 (1H, s). Anal. Calcd for C15H14F3N3O4: C, 50.42; H, 3.95; N, 11.76. Found: C, 50.48; H, 4.07; N, 11.66.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513251B2
Source datasetuspto-grants-2013_08
ORD IDord-0c99112f1f07431fbc78c64ae0d03e73
Source noteuspto-grants-2013_08