7-(3-(benzyloxy)phenyl)-5-methyl-2-((4-methyl-1,4-diazepan-1-yl)methyl)thieno[3,2-c]pyridin-4(5H)-one hydrochloride

Base Information

Chemical Name:7-(3-(benzyloxy)phenyl)-5-methyl-2-((4-methyl-1,4-diazepan-1-yl)methyl)thieno[3,2-c]pyridin-4(5H)-one hydrochloride
CAS No.:1610521-72-6
Molecular Formula:C₂₈H₃₁N₃O₂S
Molecular Weight:473.639
Hs Code.:

Synonyms:7-(3-(benzyloxy)phenyl)-5-methyl-2-((4-methyl-1,4-diazepan-1-yl)methyl)thieno[3,2-c]pyridin-4(5H)-one hydrochloride

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Chemical Property of 7-(3-(benzyloxy)phenyl)-5-methyl-2-((4-methyl-1,4-diazepan-1-yl)methyl)thieno[3,2-c]pyridin-4(5H)-one hydrochloride

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Technology Process of 7-(3-(benzyloxy)phenyl)-5-methyl-2-((4-methyl-1,4-diazepan-1-yl)methyl)thieno[3,2-c]pyridin-4(5H)-one hydrochloride

There total 5 articles about 7-(3-(benzyloxy)phenyl)-5-methyl-2-((4-methyl-1,4-diazepan-1-yl)methyl)thieno[3,2-c]pyridin-4(5H)-one hydrochloride 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: 40.0%

: 1610520-82-5
7-bromo-5-methyl-2-((4-methyl-1,4-diazepan-1-yl)methyl)thieno[3,2-c]pyridin-4(5H)-one

: 156682-54-1
3-(benzyloxy)phenylboronic acid

: 1610521-72-6
7-(3-(benzyloxy)phenyl)-5-methyl-2-((4-methyl-1,4-diazepan-1-yl)methyl)thieno[3,2-c]pyridin-4(5H)-one hydrochloride

Guidance literature:: 7-bromo-5-methyl-2-((4-methyl-1,4-diazepan-1-yl)methyl)thieno[3,2-c]pyridin-4(5H)-one; 3-(benzyloxy)phenylboronic acid; With [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride; potassium carbonate; In water; isopropyl alcohol; at 130 ℃; for 0.5h; Microwave irradiation;

With hydrogenchloride; In diethyl ether; ethyl acetate;

Reference yield:

: 28948-60-9
2-bromothieno[3,2-c]pyridin-4(5H)-one

: 1610521-72-6
7-(3-(benzyloxy)phenyl)-5-methyl-2-((4-methyl-1,4-diazepan-1-yl)methyl)thieno[3,2-c]pyridin-4(5H)-one hydrochloride

Guidance literature:: Multi-step reaction with 5 steps

1.1: n-butyllithium / tetrahydrofuran; hexane / 2.5 h / -78 - -60 °C / Inert atmosphere

1.2: 1 h / -60 - 20 °C / Inert atmosphere

2.1: N-Bromosuccinimide / tetrahydrofuran / 24 h / 20 °C

3.1: caesium carbonate / tetrahydrofuran / 0.33 h / 20 °C

3.2: 20 °C

4.1: acetic acid / dichloromethane / 0.25 h / 40 °C

4.2: 1 h / 40 °C / Inert atmosphere

5.1: potassium carbonate; [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride / water; isopropyl alcohol / 0.5 h / 130 °C / Microwave irradiation

With N-Bromosuccinimide; n-butyllithium; [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride; potassium carbonate; caesium carbonate; acetic acid; In tetrahydrofuran; hexane; dichloromethane; water; isopropyl alcohol;

Reference yield:

: 1610520-27-8
4-oxo-4,5-dihydrothieno[3,2-c]pyridine-2-carbaldehyde

: 1610521-72-6
7-(3-(benzyloxy)phenyl)-5-methyl-2-((4-methyl-1,4-diazepan-1-yl)methyl)thieno[3,2-c]pyridin-4(5H)-one hydrochloride

Guidance literature:: Multi-step reaction with 4 steps

1.1: N-Bromosuccinimide / tetrahydrofuran / 24 h / 20 °C

2.1: caesium carbonate / tetrahydrofuran / 0.33 h / 20 °C

2.2: 20 °C

3.1: acetic acid / dichloromethane / 0.25 h / 40 °C

3.2: 1 h / 40 °C / Inert atmosphere

4.1: potassium carbonate; [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride / water; isopropyl alcohol / 0.5 h / 130 °C / Microwave irradiation

With N-Bromosuccinimide; [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride; potassium carbonate; caesium carbonate; acetic acid; In tetrahydrofuran; dichloromethane; water; isopropyl alcohol;