3-amino-4-(4-chlorophenyl)-6,7-dihydro-5H-cyclopenta[e]thieno[2,3-b]pyridine-2-carboxylic acid

Base Information

Chemical Name:3-amino-4-(4-chlorophenyl)-6,7-dihydro-5H-cyclopenta[e]thieno[2,3-b]pyridine-2-carboxylic acid
CAS No.:906375-55-1
Molecular Formula:C₁₇H₁₃ClN₂O₂S
Molecular Weight:344.821
Hs Code.:

Synonyms:3-amino-4-(4-chlorophenyl)-6,7-dihydro-5H-cyclopenta[e]thieno[2,3-b]pyridine-2-carboxylic acid

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Chemical Property of 3-amino-4-(4-chlorophenyl)-6,7-dihydro-5H-cyclopenta[e]thieno[2,3-b]pyridine-2-carboxylic acid

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Technology Process of 3-amino-4-(4-chlorophenyl)-6,7-dihydro-5H-cyclopenta[e]thieno[2,3-b]pyridine-2-carboxylic acid

There total 3 articles about 3-amino-4-(4-chlorophenyl)-6,7-dihydro-5H-cyclopenta[e]thieno[2,3-b]pyridine-2-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: 82.0%

: 434293-29-5
3-amino-4-(4-chloro-phenyl)-6,7-dihydro-5H-1-thia-8-aza-s-indacene-2-carboxylic acid ethyl ester

: 906375-55-1
3-amino-4-(4-chlorophenyl)-6,7-dihydro-5H-cyclopenta[e]thieno[2,3-b]pyridine-2-carboxylic acid

Guidance literature:: With sodium hydroxide; In ethanol; for 4h; Heating;
DOI:10.1002/jccs.200500136

Reference yield:

: 83236-50-4
4-<4-chlorophenyl>-3-cyano-5,6-trimethylenepyridine-2<1H>-thione

: 906375-55-1
3-amino-4-(4-chlorophenyl)-6,7-dihydro-5H-cyclopenta[e]thieno[2,3-b]pyridine-2-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 88 percent / sodium acetate trihydrate / ethanol / 2 h / Heating

2: 90 percent / sodium ethoxide / ethanol / 0.08 h / Heating

3: 82 percent / sodium hydroxide / ethanol / 4 h / Heating

With sodium hydroxide; sodium ethanolate; sodium acetate; In ethanol; 2: Thorpe-Ziegler cyclisation;
DOI:10.1002/jccs.200500136

Reference yield:

: 536720-16-8
[4-(4-chloro-phenyl)-3-cyano-6,7-dihydro-5H-[1]pyrindin-2-ylsulfanyl]-acetic acid ethyl ester

: 906375-55-1
3-amino-4-(4-chlorophenyl)-6,7-dihydro-5H-cyclopenta[e]thieno[2,3-b]pyridine-2-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / sodium ethoxide / ethanol / 0.08 h / Heating

2: 82 percent / sodium hydroxide / ethanol / 4 h / Heating

With sodium hydroxide; sodium ethanolate; In ethanol; 1: Thorpe-Ziegler cyclisation;
DOI:10.1002/jccs.200500136