(E)-ethyl 6-benzyl-2-(((phenylamino)(pyrrolidin-1-yl)methylene)amino)-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxylate

Base Information

Chemical Name:(E)-ethyl 6-benzyl-2-(((phenylamino)(pyrrolidin-1-yl)methylene)amino)-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxylate
CAS No.:1609274-95-4
Molecular Formula:C₂₈H₃₂N₄O₂S
Molecular Weight:488.654
Hs Code.:

Synonyms:(E)-ethyl 6-benzyl-2-(((phenylamino)(pyrrolidin-1-yl)methylene)amino)-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxylate

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Chemical Property of (E)-ethyl 6-benzyl-2-(((phenylamino)(pyrrolidin-1-yl)methylene)amino)-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxylate

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Technology Process of (E)-ethyl 6-benzyl-2-(((phenylamino)(pyrrolidin-1-yl)methylene)amino)-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxylate

There total 5 articles about (E)-ethyl 6-benzyl-2-(((phenylamino)(pyrrolidin-1-yl)methylene)amino)-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxylate 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:

: 123-75-1
pyrrolidine

: 1340480-83-2
C₂₄H₂₃N₃O₂S

: 1609274-95-4
(E)-ethyl 6-benzyl-2-(((phenylamino)(pyrrolidin-1-yl)methylene)amino)-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxylate

Guidance literature:: pyrrolidine; C₂₄H₂₃N₃O₂S; In dichloromethane; at 20 ℃;

With sodium ethanolate; In ethanol; at 60 ℃; for 6h;
DOI:10.1080/00397911.2013.859705

Reference yield:

: 3612-20-2
1-phenylmethyl-4-piperidone

: 1609274-95-4
(E)-ethyl 6-benzyl-2-(((phenylamino)(pyrrolidin-1-yl)methylene)amino)-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: sulfur; triethylamine / N,N-dimethyl-formamide / 5 h / 20 °C

2.1: triethylamine; hexachloroethane / 6 h / 0 - 5 °C

3.1: dichloromethane / 20 °C / Inert atmosphere

4.1: dichloromethane / 20 °C

4.2: 6 h / 60 °C

With hexachloroethane; sulfur; triethylamine; In dichloromethane; N,N-dimethyl-formamide; 1.1: |Gewald Aminoheterocycles Synthesis;
DOI:10.1080/00397911.2013.859705

Reference yield:

: 105-56-6
ethyl 2-cyanoacetate

: 1609274-95-4
(E)-ethyl 6-benzyl-2-(((phenylamino)(pyrrolidin-1-yl)methylene)amino)-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: sulfur; triethylamine / N,N-dimethyl-formamide / 5 h / 20 °C

2.1: triethylamine; hexachloroethane / 6 h / 0 - 5 °C

3.1: dichloromethane / 20 °C / Inert atmosphere

4.1: dichloromethane / 20 °C

4.2: 6 h / 60 °C

With hexachloroethane; sulfur; triethylamine; In dichloromethane; N,N-dimethyl-formamide; 1.1: |Gewald Aminoheterocycles Synthesis;
DOI:10.1080/00397911.2013.859705