methyl 5-methoxy-4-oxo-1-[3-(trifluoromethyl)phenyl]-1,4-dihydropyridazine-3-carboxylate

Base Information

Chemical Name:methyl 5-methoxy-4-oxo-1-[3-(trifluoromethyl)phenyl]-1,4-dihydropyridazine-3-carboxylate
CAS No.:1238701-62-6
Molecular Formula:C₁₄H₁₁F₃N₂O₄
Molecular Weight:328.248
Hs Code.:

Synonyms:methyl 5-methoxy-4-oxo-1-[3-(trifluoromethyl)phenyl]-1,4-dihydropyridazine-3-carboxylate

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Chemical Property of methyl 5-methoxy-4-oxo-1-[3-(trifluoromethyl)phenyl]-1,4-dihydropyridazine-3-carboxylate

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Technology Process of methyl 5-methoxy-4-oxo-1-[3-(trifluoromethyl)phenyl]-1,4-dihydropyridazine-3-carboxylate

There total 3 articles about methyl 5-methoxy-4-oxo-1-[3-(trifluoromethyl)phenyl]-1,4-dihydropyridazine-3-carboxylate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 89.0%

: 1238701-59-1
methyl 4-methoxy-3-oxo-2-{[3-(trifluoromethyl)phenyl]hydrazono}butanoate

: 4637-24-5
N,N-dimethyl-formamide dimethyl acetal

: 1238701-62-6
methyl 5-methoxy-4-oxo-1-[3-(trifluoromethyl)phenyl]-1,4-dihydropyridazine-3-carboxylate

Guidance literature:: for 4h; Reflux;

Reference yield:

: 98-16-8
3-trifluoromethylaniline

: 1238701-62-6
methyl 5-methoxy-4-oxo-1-[3-(trifluoromethyl)phenyl]-1,4-dihydropyridazine-3-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium nitrite; hydrogenchloride / water / 0.25 h / 0 °C

1.2: 0 °C

2.1: 4 h / Reflux

With hydrogenchloride; sodium nitrite; In water;
DOI:10.1021/jm5013648

Reference yield:

: 41051-15-4
4-methoxyacetoacetic acid methylester

: 1238701-62-6
methyl 5-methoxy-4-oxo-1-[3-(trifluoromethyl)phenyl]-1,4-dihydropyridazine-3-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium nitrite; hydrogenchloride / water / 0.25 h / 0 °C

1.2: 0 °C

2.1: 4 h / Reflux

With hydrogenchloride; sodium nitrite; In water;
DOI:10.1021/jm5013648