1-((6-(7-(2-(4-chlorophenylamino)benzo[d]oxazol-5-yloxy)thieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl)pyrrolidin-2-one

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Chemical Name:1-((6-(7-(2-(4-chlorophenylamino)benzo[d]oxazol-5-yloxy)thieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl)pyrrolidin-2-one
CAS No.:1430330-92-9
Molecular Formula:C₃₀H₂₂ClN₅O₃S
Molecular Weight:568.055
Hs Code.:

Synonyms:1-((6-(7-(2-(4-chlorophenylamino)benzo[d]oxazol-5-yloxy)thieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl)pyrrolidin-2-one

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Chemical Property of 1-((6-(7-(2-(4-chlorophenylamino)benzo[d]oxazol-5-yloxy)thieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl)pyrrolidin-2-one

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Technology Process of 1-((6-(7-(2-(4-chlorophenylamino)benzo[d]oxazol-5-yloxy)thieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl)pyrrolidin-2-one

There total 7 articles about 1-((6-(7-(2-(4-chlorophenylamino)benzo[d]oxazol-5-yloxy)thieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl)pyrrolidin-2-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: 12.0%

: 1430331-39-7
2-(4-chlorophenylamino)benzo[d]oxazol-5-ol

: 1430331-72-8
1-((6-(7-chlorothieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl)pyrrolidin-2-one

: 1430330-92-9
1-((6-(7-(2-(4-chlorophenylamino)benzo[d]oxazol-5-yloxy)thieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl)pyrrolidin-2-one

Guidance literature:: With potassium tert-butylate; In dimethyl sulfoxide; at 20 - 80 ℃; for 2.5h; Inert atmosphere;

Reference yield:

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

: 1430330-92-9
1-((6-(7-(2-(4-chlorophenylamino)benzo[d]oxazol-5-yloxy)thieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl)pyrrolidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

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

2: potassium tert-butylate / dimethyl sulfoxide / 2.5 h / 20 - 80 °C / Inert atmosphere

With methanol; potassium tert-butylate; potassium carbonate; In tetrahydrofuran; dimethyl sulfoxide;

Reference yield:

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

: 1430330-92-9
1-((6-(7-(2-(4-chlorophenylamino)benzo[d]oxazol-5-yloxy)thieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl)pyrrolidin-2-one

Guidance literature:: Multi-step reaction with 3 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 / 2.5 h / 20 - 80 °C / Inert atmosphere

With methanol; potassium tert-butylate; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; dimethyl sulfoxide;