N-[2-(5-methyl-4,5,6,7-tetrahydro[1,3]thiazolo[5,4-c]pyridin-2-ylcarbamoyl)benzyl]-5-chlorothiophene-2-carboxamide

Base Information

Chemical Name:N-[2-(5-methyl-4,5,6,7-tetrahydro[1,3]thiazolo[5,4-c]pyridin-2-ylcarbamoyl)benzyl]-5-chlorothiophene-2-carboxamide
CAS No.:1057855-68-1
Molecular Formula:C₂₀H₁₉ClN₄O₂S₂
Molecular Weight:446.981
Hs Code.:

Synonyms:N-[2-(5-methyl-4,5,6,7-tetrahydro[1,3]thiazolo[5,4-c]pyridin-2-ylcarbamoyl)benzyl]-5-chlorothiophene-2-carboxamide

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Chemical Property of N-[2-(5-methyl-4,5,6,7-tetrahydro[1,3]thiazolo[5,4-c]pyridin-2-ylcarbamoyl)benzyl]-5-chlorothiophene-2-carboxamide

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Technology Process of N-[2-(5-methyl-4,5,6,7-tetrahydro[1,3]thiazolo[5,4-c]pyridin-2-ylcarbamoyl)benzyl]-5-chlorothiophene-2-carboxamide

There total 6 articles about N-[2-(5-methyl-4,5,6,7-tetrahydro[1,3]thiazolo[5,4-c]pyridin-2-ylcarbamoyl)benzyl]-5-chlorothiophene-2-carboxamide 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: 80.0%

: 50-00-0,30525-89-4,61233-19-0
formaldehyd

: 1057855-67-0
N-[2-(4,5,6,7-tetrahydro[1,3]thiazolo[5,4-c]pyridin-2-ylcarbamoyl)benzyl]-5-chlorothiophene-2-carboxamide

: 1057855-68-1
N-[2-(5-methyl-4,5,6,7-tetrahydro[1,3]thiazolo[5,4-c]pyridin-2-ylcarbamoyl)benzyl]-5-chlorothiophene-2-carboxamide

Guidance literature:: With sodium tris(acetoxy)borohydride; acetic acid; In dichloromethane; water; for 6.08333h;
DOI:10.1016/j.bmc.2011.01.035

Reference yield:

: 24065-33-6
5-Chlorothiophene-2-carboxylic acid

: 1057855-68-1
N-[2-(5-methyl-4,5,6,7-tetrahydro[1,3]thiazolo[5,4-c]pyridin-2-ylcarbamoyl)benzyl]-5-chlorothiophene-2-carboxamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 28 h / 20 °C

2.1: aluminum (III) chloride; dimethylsulfide / dichloromethane / 2 h / 20 °C

2.2: ice

3.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 24 h / 20 °C

4.1: hydrogenchloride / 1,4-dioxane / 2.67 h / 20 - 50 °C

5.1: sodium hydrogencarbonate / water

6.1: sodium tris(acetoxy)borohydride; acetic acid / dichloromethane; water / 6.08 h

With hydrogenchloride; aluminum (III) chloride; dimethylsulfide; sodium tris(acetoxy)borohydride; sodium hydrogencarbonate; benzotriazol-1-ol; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In 1,4-dioxane; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2011.01.035

Reference yield:

: 1057653-07-2
methyl 2-{[(5-chlorothiophen-2-yl)carbonylamino]methyl}benzoate

: 1057855-68-1
N-[2-(5-methyl-4,5,6,7-tetrahydro[1,3]thiazolo[5,4-c]pyridin-2-ylcarbamoyl)benzyl]-5-chlorothiophene-2-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: aluminum (III) chloride; dimethylsulfide / dichloromethane / 2 h / 20 °C

1.2: ice

2.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 24 h / 20 °C

3.1: hydrogenchloride / 1,4-dioxane / 2.67 h / 20 - 50 °C

4.1: sodium hydrogencarbonate / water

5.1: sodium tris(acetoxy)borohydride; acetic acid / dichloromethane; water / 6.08 h

With hydrogenchloride; aluminum (III) chloride; dimethylsulfide; sodium tris(acetoxy)borohydride; sodium hydrogencarbonate; benzotriazol-1-ol; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In 1,4-dioxane; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2011.01.035