HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1805451Generated: October 31, 2026
Methanamine, N-methoxy-, hydrochloride (1:1) → HCID 59436282, compound
https://huagongshe.com/reaction/1805451
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | HCID 59436265 | HCID 59436265 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59436282 | HCID 59436282 | 98% |
Reaction Steps
To a stirred suspension of N,O-dimethylhydroxylamine hydrochloride (0.468 g, 4.8 mmol) in dichloromethane (5 mL) was added trimethylaluminum (2.4 mL, 4.8 mmol, 2 M solution in toluene) dropwise at 0° C. Following addition, the suspension was stirred at 0° C. for 10 min then at room temperature for 30 min to provide a homogenous solution. The flask was then re-cooled in an ice bath. In a separate flask, methyl 5-methyl-4-oxo-1-[3-(trifluoromethyl)phenyl]-1,4-dihydropyridazine-3-carboxylate (0.500 g, 1.6 mmol) was dissolved in dichloromethane (5 mL) and added dropwise and allowed to stir for 2 h. The reaction was quenched with water (5 mL) and 2 N HCl aqueous solution (2 mL). The layers were separated and the aqueous layer was extracted with dichloromethane (2×10 mL). The combined organic extracts were washed with brine (20 mL), dried (Na2SO4), filtered and concentrated to provide N-methoxy-N,5-dimethyl-4-oxo-1-[3-(trifluoromethyl)phenyl]-1,4-dihydropyridazine-3-carboxamide (0.535 g, 98%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08354411B2 |
|---|
| Source dataset | uspto-grants-2013_01 |
|---|
| ORD ID | ord-9bef8c7adfd049a2b8827bad9f12038c |
|---|
| Source note | uspto-grants-2013_01 |
|---|