tert-butyl (2-(7-(2-fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)-1-methyl-1H-imidazol-5-yl)methyl(2-methoxyethyl)carbamate

Base Information

Chemical Name:tert-butyl (2-(7-(2-fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)-1-methyl-1H-imidazol-5-yl)methyl(2-methoxyethyl)carbamate
CAS No.:1127329-24-1
Molecular Formula:C₂₆H₂₈FN₅O₆S
Molecular Weight:557.603
Hs Code.:

Synonyms:tert-butyl (2-(7-(2-fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)-1-methyl-1H-imidazol-5-yl)methyl(2-methoxyethyl)carbamate

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Chemical Property of tert-butyl (2-(7-(2-fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)-1-methyl-1H-imidazol-5-yl)methyl(2-methoxyethyl)carbamate

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Technology Process of tert-butyl (2-(7-(2-fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)-1-methyl-1H-imidazol-5-yl)methyl(2-methoxyethyl)carbamate

There total 8 articles about tert-butyl (2-(7-(2-fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)-1-methyl-1H-imidazol-5-yl)methyl(2-methoxyethyl)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: 71.0%

: 1127329-23-0
N-((2-(7-(2-fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)-1-methyl-1H-imidazol-5-yl)methyl)-2-methoxyethanamine

: 24424-99-5
di-tert-butyl dicarbonate

: 1127329-24-1
tert-butyl (2-(7-(2-fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)-1-methyl-1H-imidazol-5-yl)methyl(2-methoxyethyl)carbamate

Guidance literature:: In dichloromethane; at 20 ℃;

Reference yield:

: 39021-62-0
1-methylimidazole-5-carbaldehyde

: 1127329-24-1
tert-butyl (2-(7-(2-fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)-1-methyl-1H-imidazol-5-yl)methyl(2-methoxyethyl)carbamate

Guidance literature:: Multi-step reaction with 8 steps

1.1: camphor-10-sulfonic acid / toluene / 24 h / Reflux

2.1: n-butyllithium / tetrahydrofuran; hexanes / 0.33 h / -78 °C

2.2: -78 °C

3.1: n-butyllithium / tetrahydrofuran; hexanes / 0.17 h / -78 °C

3.2: -78 - 20 °C

3.3: 4 h / Reflux; Inert atmosphere

4.1: sodium hydrogencarbonate / diphenylether / 4 h / 180 °C

5.1: camphor-10-sulfonic acid / 5 h / Reflux

6.1: hydrogenchloride; water / acetone / 20 °C

7.1: sodium tris(acetoxy)borohydride; acetic acid / dichloromethane / 24 h / 20 °C

8.1: dichloromethane / 20 °C

With hydrogenchloride; n-butyllithium; water; sodium tris(acetoxy)borohydride; sodium hydrogencarbonate; acetic acid; camphor-10-sulfonic acid; In tetrahydrofuran; hexanes; diphenylether; dichloromethane; acetone; toluene;

Reference yield:

: 1127329-18-3
5-(1,3-dioxan-2-yl)-2-iodo-1-methyl-1H-imidazole

: 1127329-24-1
tert-butyl (2-(7-(2-fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)-1-methyl-1H-imidazol-5-yl)methyl(2-methoxyethyl)carbamate

Guidance literature:: Multi-step reaction with 6 steps

1.1: n-butyllithium / tetrahydrofuran; hexanes / 0.17 h / -78 °C

1.2: -78 - 20 °C

1.3: 4 h / Reflux; Inert atmosphere

2.1: sodium hydrogencarbonate / diphenylether / 4 h / 180 °C

3.1: camphor-10-sulfonic acid / 5 h / Reflux

4.1: hydrogenchloride; water / acetone / 20 °C

5.1: sodium tris(acetoxy)borohydride; acetic acid / dichloromethane / 24 h / 20 °C

6.1: dichloromethane / 20 °C

With hydrogenchloride; n-butyllithium; water; sodium tris(acetoxy)borohydride; sodium hydrogencarbonate; acetic acid; camphor-10-sulfonic acid; In tetrahydrofuran; hexanes; diphenylether; dichloromethane; acetone;