N-(4-chlorophenyl)-5-(2-(5-((prop-2-ynylamino)methyl)pyridin-2-yl)thieno[3,2-b]pyridin-7-yloxy)benzo[d]oxazol-2-amine

Base Information

Chemical Name:N-(4-chlorophenyl)-5-(2-(5-((prop-2-ynylamino)methyl)pyridin-2-yl)thieno[3,2-b]pyridin-7-yloxy)benzo[d]oxazol-2-amine
CAS No.:1430331-49-9
Molecular Formula:C₂₉H₂₀ClN₅O₂S
Molecular Weight:538.029
Hs Code.:

Synonyms:N-(4-chlorophenyl)-5-(2-(5-((prop-2-ynylamino)methyl)pyridin-2-yl)thieno[3,2-b]pyridin-7-yloxy)benzo[d]oxazol-2-amine

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Chemical Property of N-(4-chlorophenyl)-5-(2-(5-((prop-2-ynylamino)methyl)pyridin-2-yl)thieno[3,2-b]pyridin-7-yloxy)benzo[d]oxazol-2-amine

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Technology Process of N-(4-chlorophenyl)-5-(2-(5-((prop-2-ynylamino)methyl)pyridin-2-yl)thieno[3,2-b]pyridin-7-yloxy)benzo[d]oxazol-2-amine

There total 7 articles about N-(4-chlorophenyl)-5-(2-(5-((prop-2-ynylamino)methyl)pyridin-2-yl)thieno[3,2-b]pyridin-7-yloxy)benzo[d]oxazol-2-amine 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: 73.0%

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

: 2450-71-7
Propargylamine

: 1430331-49-9
N-(4-chlorophenyl)-5-(2-(5-((prop-2-ynylamino)methyl)pyridin-2-yl)thieno[3,2-b]pyridin-7-yloxy)benzo[d]oxazol-2-amine

Guidance literature:: With phenylsilane; dibutyltin chloride; In ethyl acetate; N,N-dimethyl-formamide; at 20 ℃;

Reference yield:

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

: 1430331-49-9
N-(4-chlorophenyl)-5-(2-(5-((prop-2-ynylamino)methyl)pyridin-2-yl)thieno[3,2-b]pyridin-7-yloxy)benzo[d]oxazol-2-amine

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 / ethyl acetate; N,N-dimethyl-formamide / 20 °C

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

Reference yield:

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

: 1430331-49-9
N-(4-chlorophenyl)-5-(2-(5-((prop-2-ynylamino)methyl)pyridin-2-yl)thieno[3,2-b]pyridin-7-yloxy)benzo[d]oxazol-2-amine

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 / ethyl acetate; N,N-dimethyl-formamide / 20 °C

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