2-(5-(3,5-difluorophenoxy)-2,3,4,5-tetrahydro-1H-benzo[c]azepin-8-yl)pyridazin-3(2H)-one

Base Information

Chemical Name:2-(5-(3,5-difluorophenoxy)-2,3,4,5-tetrahydro-1H-benzo[c]azepin-8-yl)pyridazin-3(2H)-one
CAS No.:1084810-40-1
Molecular Formula:C₂₀H₁₇F₂N₃O₂
Molecular Weight:369.371
Hs Code.:

Synonyms:2-(5-(3,5-difluorophenoxy)-2,3,4,5-tetrahydro-1H-benzo[c]azepin-8-yl)pyridazin-3(2H)-one

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Chemical Property of 2-(5-(3,5-difluorophenoxy)-2,3,4,5-tetrahydro-1H-benzo[c]azepin-8-yl)pyridazin-3(2H)-one

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Technology Process of 2-(5-(3,5-difluorophenoxy)-2,3,4,5-tetrahydro-1H-benzo[c]azepin-8-yl)pyridazin-3(2H)-one

There total 7 articles about 2-(5-(3,5-difluorophenoxy)-2,3,4,5-tetrahydro-1H-benzo[c]azepin-8-yl)pyridazin-3(2H)-one 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: 17.0%

: 1084810-36-5
2-(5-(3,5-difluorophenoxy)-2-methyl-2,3,4,5-tetrahydro-1H-benzo[c]azepin-8-yl)pyridazin-3(2H)-one

: 1084810-40-1
2-(5-(3,5-difluorophenoxy)-2,3,4,5-tetrahydro-1H-benzo[c]azepin-8-yl)pyridazin-3(2H)-one

Guidance literature:: 2-(5-(3,5-difluorophenoxy)-2-methyl-2,3,4,5-tetrahydro-1H-benzo[c]azepin-8-yl)pyridazin-3(2H)-one; With carbonochloridic acid 1-chloro-ethyl ester; N,N,N',N'-tetramethyl-1,8-diaminonaphthalene; In 1,2-dichloro-ethane; at 0 ℃; for 3h;

With methanol; for 2h; Heating / reflux;

With sodium hydrogencarbonate; In dichloromethane; water;

Reference yield:

: 3132-99-8
m-bromobenzoic aldehyde

: 1084810-40-1
2-(5-(3,5-difluorophenoxy)-2,3,4,5-tetrahydro-1H-benzo[c]azepin-8-yl)pyridazin-3(2H)-one

Guidance literature:: Multi-step reaction with 7 steps

1.1: iodine / methanol; water / 0.5 h / 0 °C

1.2: 5 h / 0 °C

2.1: pyridine / 2 h / Heating / reflux

3.1: trifluorormethanesulfonic acid / 72 h / 120 °C

3.2: 0 °C / pH 9

4.1: sodium tetrahydroborate / methanol / 1 h / 0 °C

5.1: tributylphosphine; 1,1'-azodicarbonyl-dipiperidine / tetrahydrofuran / 1.5 h / 20 °C

6.1: potassium phosphate; N,N`-dimethylethylenediamine / copper(l) iodide / 1,4-dioxane / 16 h / 110 °C

7.1: carbonochloridic acid 1-chloro-ethyl ester; N,N,N',N'-tetramethyl-1,8-diaminonaphthalene / 1,2-dichloro-ethane / 3 h / 0 °C

7.2: 2 h / Heating / reflux

With pyridine; sodium tetrahydroborate; potassium phosphate; tributylphosphine; carbonochloridic acid 1-chloro-ethyl ester; trifluorormethanesulfonic acid; iodine; N,N,N',N'-tetramethyl-1,8-diaminonaphthalene; N,N`-dimethylethylenediamine; 1,1'-azodicarbonyl-dipiperidine; copper(l) iodide; In tetrahydrofuran; 1,4-dioxane; methanol; water; 1,2-dichloro-ethane;

Reference yield:

: 1084811-94-8
C₁₁H₁₄BrNO₂

: 1084810-40-1
2-(5-(3,5-difluorophenoxy)-2,3,4,5-tetrahydro-1H-benzo[c]azepin-8-yl)pyridazin-3(2H)-one

Guidance literature:: Multi-step reaction with 5 steps

1.1: trifluorormethanesulfonic acid / 72 h / 120 °C

1.2: 0 °C / pH 9

2.1: sodium tetrahydroborate / methanol / 1 h / 0 °C

3.1: tributylphosphine; 1,1'-azodicarbonyl-dipiperidine / tetrahydrofuran / 1.5 h / 20 °C

4.1: potassium phosphate; N,N`-dimethylethylenediamine / copper(l) iodide / 1,4-dioxane / 16 h / 110 °C

5.1: carbonochloridic acid 1-chloro-ethyl ester; N,N,N',N'-tetramethyl-1,8-diaminonaphthalene / 1,2-dichloro-ethane / 3 h / 0 °C

5.2: 2 h / Heating / reflux

With sodium tetrahydroborate; potassium phosphate; tributylphosphine; carbonochloridic acid 1-chloro-ethyl ester; trifluorormethanesulfonic acid; N,N,N',N'-tetramethyl-1,8-diaminonaphthalene; N,N`-dimethylethylenediamine; 1,1'-azodicarbonyl-dipiperidine; copper(l) iodide; In tetrahydrofuran; 1,4-dioxane; methanol; 1,2-dichloro-ethane;