methyl 3-(4-(2-(5-((tert-butoxycarbonyl(2-methoxyemyl)amino)methyl)pyridin-2-yl)thieno[3,2-b]pyridin-7-yloxy)-3-fluorophenylamino)-3-oxopropanoate

Base Information

Chemical Name:methyl 3-(4-(2-(5-((tert-butoxycarbonyl(2-methoxyemyl)amino)methyl)pyridin-2-yl)thieno[3,2-b]pyridin-7-yloxy)-3-fluorophenylamino)-3-oxopropanoate
CAS No.:1187214-04-5
Molecular Formula:C₃₁H₃₃FN₄O₇S
Molecular Weight:624.69
Hs Code.:

methyl 3-(4-(2-(5-((tert-butoxycarbonyl(2-methoxyemyl)amino)methyl)pyridin-2-yl)thieno[3,2-b]pyridin-7-yloxy)-3-fluorophenylamino)-3-oxopropanoate

Synonyms:methyl 3-(4-(2-(5-((tert-butoxycarbonyl(2-methoxyemyl)amino)methyl)pyridin-2-yl)thieno[3,2-b]pyridin-7-yloxy)-3-fluorophenylamino)-3-oxopropanoate

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Chemical Property of methyl 3-(4-(2-(5-((tert-butoxycarbonyl(2-methoxyemyl)amino)methyl)pyridin-2-yl)thieno[3,2-b]pyridin-7-yloxy)-3-fluorophenylamino)-3-oxopropanoate

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Technology Process of methyl 3-(4-(2-(5-((tert-butoxycarbonyl(2-methoxyemyl)amino)methyl)pyridin-2-yl)thieno[3,2-b]pyridin-7-yloxy)-3-fluorophenylamino)-3-oxopropanoate

There total 5 articles about methyl 3-(4-(2-(5-((tert-butoxycarbonyl(2-methoxyemyl)amino)methyl)pyridin-2-yl)thieno[3,2-b]pyridin-7-yloxy)-3-fluorophenylamino)-3-oxopropanoate 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: 94.0%

: 37517-81-0
3-chloro-3-oxopropanoic acid methyl ester

: 1123837-34-2
tert-butyl {[6-[7-(4-amino-2-fluorophenoxy)thieno[3,2-b]pyridin-2-yl]pyridin-3-yl]methyl}(2-methoxyethyl)carbamate

: 1187214-04-5
methyl 3-(4-(2-(5-((tert-butoxycarbonyl(2-methoxyemyl)amino)methyl)pyridin-2-yl)thieno[3,2-b]pyridin-7-yloxy)-3-fluorophenylamino)-3-oxopropanoate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 18h;

Reference yield:

: 1123837-99-9
N-((6-bromopyridin-3-yl)methyl)-2-methoxyethan-1-amine

: 1187214-04-5
methyl 3-(4-(2-(5-((tert-butoxycarbonyl(2-methoxyemyl)amino)methyl)pyridin-2-yl)thieno[3,2-b]pyridin-7-yloxy)-3-fluorophenylamino)-3-oxopropanoate

Guidance literature:: Multi-step reaction with 4 steps

1.1: tetrahydrofuran / 16 h / 20 °C

2.1: n-butyllithium / tetrahydrofuran / 0.5 h / -78 °C

2.2: 1 h / -78 - 20 °C

2.3: 1 h / Reflux

3.1: potassium tert-butylate / dimethyl sulfoxide / 0.5 h

3.2: 0.75 h / 100 °C

4.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 18 h / 20 °C

With n-butyllithium; potassium tert-butylate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; dimethyl sulfoxide;

Reference yield:

: 1123838-02-7
tert-butyl {[6-(7-chlorothieno[3,2-b]pyridin-2-yl)pyridin-3-yl]methyl}(2-methoxyethyl)carbamate

: 1187214-04-5
methyl 3-(4-(2-(5-((tert-butoxycarbonyl(2-methoxyemyl)amino)methyl)pyridin-2-yl)thieno[3,2-b]pyridin-7-yloxy)-3-fluorophenylamino)-3-oxopropanoate

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium tert-butylate / dimethyl sulfoxide / 0.5 h

1.2: 0.75 h / 100 °C

2.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 18 h / 20 °C

With potassium tert-butylate; N-ethyl-N,N-diisopropylamine; In dichloromethane; dimethyl sulfoxide;