tert-butyl (6-(7-(4-(3-cyclopropylureido)-2-fluorophenoxy)thieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl(2-(2-methoxyethoxy)ethyl)carbamate

Base Information

Chemical Name:tert-butyl (6-(7-(4-(3-cyclopropylureido)-2-fluorophenoxy)thieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl(2-(2-methoxyethoxy)ethyl)carbamate
CAS No.:1187214-00-1
Molecular Formula:C₃₃H₃₈FN₅O₆S
Molecular Weight:651.759
Hs Code.:

Synonyms:tert-butyl (6-(7-(4-(3-cyclopropylureido)-2-fluorophenoxy)thieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl(2-(2-methoxyethoxy)ethyl)carbamate

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Chemical Property of tert-butyl (6-(7-(4-(3-cyclopropylureido)-2-fluorophenoxy)thieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl(2-(2-methoxyethoxy)ethyl)carbamate

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Technology Process of tert-butyl (6-(7-(4-(3-cyclopropylureido)-2-fluorophenoxy)thieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl(2-(2-methoxyethoxy)ethyl)carbamate

There total 11 articles about tert-butyl (6-(7-(4-(3-cyclopropylureido)-2-fluorophenoxy)thieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl(2-(2-methoxyethoxy)ethyl)carbamate 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:

: 32315-10-9
bis(trichloromethyl) carbonate

: 1187213-99-5
tert-butyl (6-(7-(4-amino-2-fluorophenoxy)thieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl(2-(2-methoxyethoxy)ethyl)carbamate

: 765-30-0
Cyclopropylamine

: 1187214-00-1
tert-butyl (6-(7-(4-(3-cyclopropylureido)-2-fluorophenoxy)thieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl(2-(2-methoxyethoxy)ethyl)carbamate

Guidance literature:: bis(trichloromethyl) carbonate; tert-butyl (6-(7-(4-amino-2-fluorophenoxy)thieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl(2-(2-methoxyethoxy)ethyl)carbamate; With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at 0 ℃; for 1h;

Cyclopropylamine; In tetrahydrofuran; at 0 - 20 ℃; for 18h;

Reference yield:

: 918643-34-2
6-(7-(2-fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)nicotinaldehyde

: 1187214-00-1
tert-butyl (6-(7-(4-(3-cyclopropylureido)-2-fluorophenoxy)thieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl(2-(2-methoxyethoxy)ethyl)carbamate

Guidance literature:: Multi-step reaction with 4 steps

1.1: acetic acid / dichloromethane / 1 h / 20 °C

1.2: 18 h / 20 °C

2.1: triethylamine / dmap / dichloromethane / 2 h / 20 °C

3.1: iron; ammonium chloride / methanol; water / 4 h / Reflux

4.1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 1 h / 0 °C

4.2: 18 h / 0 - 20 °C

With iron; ammonium chloride; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; dmap; In tetrahydrofuran; methanol; dichloromethane; water;

Reference yield:

: 111-77-3,95507-80-5
2-(2-methoxyethoxy)ethyl alcohol

: 1187214-00-1
tert-butyl (6-(7-(4-(3-cyclopropylureido)-2-fluorophenoxy)thieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl(2-(2-methoxyethoxy)ethyl)carbamate

Guidance literature:: Multi-step reaction with 6 steps

1.1: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 20 °C

2.1: hydrazine hydrate / ethanol / 4 h / Reflux

2.2: Reflux

3.1: acetic acid / dichloromethane / 1 h / 20 °C

3.2: 18 h / 20 °C

4.1: triethylamine / dmap / dichloromethane / 2 h / 20 °C

5.1: iron; ammonium chloride / methanol; water / 4 h / Reflux

6.1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 1 h / 0 °C

6.2: 18 h / 0 - 20 °C

With iron; ammonium chloride; hydrazine hydrate; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; triphenylphosphine; diethylazodicarboxylate; dmap; In tetrahydrofuran; methanol; ethanol; dichloromethane; water;