N-(3-fluoro-4-((6-methoxy-7-(3-(pyrrolidin-1-yl)propoxy)quinolin-4-yl)oxy)phenyl)-4-methyl-6-oxo-1-phenyl-1,6-dihydropyridazine-3-carboxamide

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Chemical Name:N-(3-fluoro-4-((6-methoxy-7-(3-(pyrrolidin-1-yl)propoxy)quinolin-4-yl)oxy)phenyl)-4-methyl-6-oxo-1-phenyl-1,6-dihydropyridazine-3-carboxamide
CAS No.:1620683-81-9
Molecular Formula:C₃₅H₃₄FN₅O₅
Molecular Weight:623.684
Hs Code.:

Synonyms:N-(3-fluoro-4-((6-methoxy-7-(3-(pyrrolidin-1-yl)propoxy)quinolin-4-yl)oxy)phenyl)-4-methyl-6-oxo-1-phenyl-1,6-dihydropyridazine-3-carboxamide

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Chemical Property of N-(3-fluoro-4-((6-methoxy-7-(3-(pyrrolidin-1-yl)propoxy)quinolin-4-yl)oxy)phenyl)-4-methyl-6-oxo-1-phenyl-1,6-dihydropyridazine-3-carboxamide

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Technology Process of N-(3-fluoro-4-((6-methoxy-7-(3-(pyrrolidin-1-yl)propoxy)quinolin-4-yl)oxy)phenyl)-4-methyl-6-oxo-1-phenyl-1,6-dihydropyridazine-3-carboxamide

There total 13 articles about N-(3-fluoro-4-((6-methoxy-7-(3-(pyrrolidin-1-yl)propoxy)quinolin-4-yl)oxy)phenyl)-4-methyl-6-oxo-1-phenyl-1,6-dihydropyridazine-3-carboxamide 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:

: 859296-96-1
4-methyl-6-oxo-1-phenyl-1,6-dihydro-pyridazine-3-carbonyl chloride

: 1394166-11-0
3-fluoro-4-((6-methoxy-7-(3-(pyrrolidin-1-yl)propoxy)quinolin-4-yl)oxy)aniline

: 1620683-81-9
N-(3-fluoro-4-((6-methoxy-7-(3-(pyrrolidin-1-yl)propoxy)quinolin-4-yl)oxy)phenyl)-4-methyl-6-oxo-1-phenyl-1,6-dihydropyridazine-3-carboxamide

Guidance literature:: With sodium carbonate; In dichloromethane; at 25 ℃; for 3h; Cooling with ice;
DOI:10.1016/j.ejmech.2014.06.068

Reference yield:

: 62-53-3
aniline

: 1620683-81-9
N-(3-fluoro-4-((6-methoxy-7-(3-(pyrrolidin-1-yl)propoxy)quinolin-4-yl)oxy)phenyl)-4-methyl-6-oxo-1-phenyl-1,6-dihydropyridazine-3-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: hydrogenchloride; sodium nitrite / water / 0.5 h / 0 °C

1.2: 0 °C

2.1: toluene / 12 h / Reflux

3.1: sodium hydroxide / tetrahydrofuran / 4 h / 50 °C

4.1: thionyl chloride / toluene / 5 h / 85 °C

5.1: sodium carbonate / dichloromethane / 3 h / 25 °C / Cooling with ice

With hydrogenchloride; thionyl chloride; sodium carbonate; sodium hydroxide; sodium nitrite; In tetrahydrofuran; dichloromethane; water; toluene;
DOI:10.1016/j.ejmech.2014.06.068

Reference yield:

: 498-02-2
1-(3-methoxy-4-hydroxyphenyl)ethanone

: 1620683-81-9
N-(3-fluoro-4-((6-methoxy-7-(3-(pyrrolidin-1-yl)propoxy)quinolin-4-yl)oxy)phenyl)-4-methyl-6-oxo-1-phenyl-1,6-dihydropyridazine-3-carboxamide

Guidance literature:: Multi-step reaction with 9 steps

1: acetone / 12.5 h / 0 - 25 °C

2: nitric acid / dichloromethane / 4 h / 0 °C

3: toluene / 10 h / 110 °C

4: iron; acetic acid / 2.5 h / 20 - 80 °C

5: acetonitrile / 10 h / 85 °C

6: trichlorophosphate / 6 h / 85 °C

7: chlorobenzene / 30 h / 140 °C

8: iron; ammonium chloride / ethanol; water / 5 h / Reflux

9: sodium carbonate / dichloromethane / 3 h / 25 °C / Cooling with ice

With nitric acid; iron; sodium carbonate; ammonium chloride; acetic acid; trichlorophosphate; In ethanol; dichloromethane; water; chlorobenzene; acetone; toluene; acetonitrile;
DOI:10.1016/j.ejmech.2014.06.068