4-((6-(7-(2-(4-chlorophenylamino)benzo[d]oxazol-5-yloxy)thieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl)amino-N-(2-(diethylamino)ethyl)benzamide

Base Information

Chemical Name:4-((6-(7-(2-(4-chlorophenylamino)benzo[d]oxazol-5-yloxy)thieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl)amino-N-(2-(diethylamino)ethyl)benzamide
CAS No.:1430330-86-1
Molecular Formula:C₃₉H₃₆ClN₇O₃S
Molecular Weight:718.279
Hs Code.:

Synonyms:4-((6-(7-(2-(4-chlorophenylamino)benzo[d]oxazol-5-yloxy)thieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl)amino-N-(2-(diethylamino)ethyl)benzamide

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Chemical Property of 4-((6-(7-(2-(4-chlorophenylamino)benzo[d]oxazol-5-yloxy)thieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl)amino-N-(2-(diethylamino)ethyl)benzamide

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Technology Process of 4-((6-(7-(2-(4-chlorophenylamino)benzo[d]oxazol-5-yloxy)thieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl)amino-N-(2-(diethylamino)ethyl)benzamide

There total 8 articles about 4-((6-(7-(2-(4-chlorophenylamino)benzo[d]oxazol-5-yloxy)thieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl)amino-N-(2-(diethylamino)ethyl)benzamide 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: 52.3%

: 1430331-42-2
6-(7-(2-(4-chlorophenylamino)benzo[d]oxazol-5-yloxy)thieno[3,2-b]pyridin-2-yl)nicotinaldehyde

: 4-amino-N-[2-(diethylamino)ethyl]benzamide hydrochloride

: 1430330-86-1
4-((6-(7-(2-(4-chlorophenylamino)benzo[d]oxazol-5-yloxy)thieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl)amino-N-(2-(diethylamino)ethyl)benzamide

Guidance literature:: With phenylsilane; dibutyltin chloride; In N,N-dimethyl-formamide; for 2.5h;

Reference yield:

: 1430331-37-5
2-(4-chlorophenylamino)benzo[d]oxazol-5-yl benzoate

: 1430330-86-1
4-((6-(7-(2-(4-chlorophenylamino)benzo[d]oxazol-5-yloxy)thieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl)amino-N-(2-(diethylamino)ethyl)benzamide

Guidance literature:: Multi-step reaction with 4 steps

1: methanol; potassium carbonate / tetrahydrofuran / 2 h / 20 °C

2: potassium tert-butylate / dimethyl sulfoxide / 1 h / 20 - 90 °C

3: hydrogenchloride / tetrahydrofuran; water / 3 h / 20 - 50 °C

4: dibutyltin chloride; phenylsilane / N,N-dimethyl-formamide / 2.5 h

With hydrogenchloride; methanol; phenylsilane; dibutyltin chloride; potassium tert-butylate; potassium carbonate; In tetrahydrofuran; water; dimethyl sulfoxide; N,N-dimethyl-formamide;

Reference yield:

: 1430331-35-3
3-(3-(4-Chlorophenyl)thioureido)-4-hydroxyphenyl benzoate

: 1430330-86-1
4-((6-(7-(2-(4-chlorophenylamino)benzo[d]oxazol-5-yloxy)thieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl)amino-N-(2-(diethylamino)ethyl)benzamide

Guidance literature:: Multi-step reaction with 5 steps

1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / Reflux

2: methanol; potassium carbonate / tetrahydrofuran / 2 h / 20 °C

3: potassium tert-butylate / dimethyl sulfoxide / 1 h / 20 - 90 °C

4: hydrogenchloride / tetrahydrofuran; water / 3 h / 20 - 50 °C

5: dibutyltin chloride; phenylsilane / N,N-dimethyl-formamide / 2.5 h

With hydrogenchloride; methanol; phenylsilane; dibutyltin chloride; potassium tert-butylate; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; water; dimethyl sulfoxide; N,N-dimethyl-formamide;