6-(2,5-difluorobenzyl)-8-(2-oxo-1,2-dihydropyridin-3-yl)-6H-thieno[2,3-e]indole-7-carboxylic acid

Base Information

Chemical Name:6-(2,5-difluorobenzyl)-8-(2-oxo-1,2-dihydropyridin-3-yl)-6H-thieno[2,3-e]indole-7-carboxylic acid
CAS No.:1037758-22-7
Molecular Formula:C₂₃H₁₄F₂N₂O₃S
Molecular Weight:436.439
Hs Code.:

Synonyms:6-(2,5-difluorobenzyl)-8-(2-oxo-1,2-dihydropyridin-3-yl)-6H-thieno[2,3-e]indole-7-carboxylic acid

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Chemical Property of 6-(2,5-difluorobenzyl)-8-(2-oxo-1,2-dihydropyridin-3-yl)-6H-thieno[2,3-e]indole-7-carboxylic acid

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Technology Process of 6-(2,5-difluorobenzyl)-8-(2-oxo-1,2-dihydropyridin-3-yl)-6H-thieno[2,3-e]indole-7-carboxylic acid

There total 8 articles about 6-(2,5-difluorobenzyl)-8-(2-oxo-1,2-dihydropyridin-3-yl)-6H-thieno[2,3-e]indole-7-carboxylic acid 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:

: 1037763-25-9
C₂₄H₁₆F₂N₂O₃S

: 1037758-22-7
6-(2,5-difluorobenzyl)-8-(2-oxo-1,2-dihydropyridin-3-yl)-6H-thieno[2,3-e]indole-7-carboxylic acid

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; methanol; at 90 ℃; for 3h;
DOI:10.1016/j.bmc.2013.01.024

Reference yield:

: 1423-61-6
7-bromobenzo(b)thiophene

: 1037758-22-7
6-(2,5-difluorobenzyl)-8-(2-oxo-1,2-dihydropyridin-3-yl)-6H-thieno[2,3-e]indole-7-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: n-butyllithium / diethyl ether; hexane / 0.33 h / -78 °C

1.2: 1 h / -78 °C

2.1: sodium methylate / methanol / 3 h / -20 - 20 °C

2.2: 0.5 h / Reflux

3.1: hydrogenchloride / methanol; 1,4-dioxane / 3 h / 90 °C

With hydrogenchloride; n-butyllithium; sodium methylate; In 1,4-dioxane; methanol; diethyl ether; hexane;
DOI:10.1016/j.bmc.2013.01.024

Reference yield:

: 10134-91-5
benzo[b]thiophene-7-carboxaldehyde

: 1037758-22-7
6-(2,5-difluorobenzyl)-8-(2-oxo-1,2-dihydropyridin-3-yl)-6H-thieno[2,3-e]indole-7-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium methylate / methanol / 3 h / -20 - 20 °C

1.2: 0.5 h / Reflux

2.1: hydrogenchloride / methanol; 1,4-dioxane / 3 h / 90 °C

With hydrogenchloride; sodium methylate; In 1,4-dioxane; methanol;
DOI:10.1016/j.bmc.2013.01.024