3,5-dimethoxy-N-(4-(1-(2-methoxyacetyl)-1H-indolin-5-yl)thiazol-2-yl)benzamide

Base Information

Chemical Name:3,5-dimethoxy-N-(4-(1-(2-methoxyacetyl)-1H-indolin-5-yl)thiazol-2-yl)benzamide
CAS No.:1604821-43-3
Molecular Formula:C₂₃H₂₃N₃O₅S
Molecular Weight:453.519
Hs Code.:

Synonyms:3,5-dimethoxy-N-(4-(1-(2-methoxyacetyl)-1H-indolin-5-yl)thiazol-2-yl)benzamide

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Chemical Property of 3,5-dimethoxy-N-(4-(1-(2-methoxyacetyl)-1H-indolin-5-yl)thiazol-2-yl)benzamide

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Technology Process of 3,5-dimethoxy-N-(4-(1-(2-methoxyacetyl)-1H-indolin-5-yl)thiazol-2-yl)benzamide

There total 8 articles about 3,5-dimethoxy-N-(4-(1-(2-methoxyacetyl)-1H-indolin-5-yl)thiazol-2-yl)benzamide 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: 79.0%

: 38870-89-2
Methoxyacetyl chloride

: 1604821-78-4
N-(4-(indolin-5-yl)thiazol-2-yl)-3,5-dimethoxybenzamide, trifluoroacetic acid salt

: 1604821-43-3
3,5-dimethoxy-N-(4-(1-(2-methoxyacetyl)-1H-indolin-5-yl)thiazol-2-yl)benzamide

Guidance literature:: With dmap; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 - 20 ℃; for 1h;

Reference yield:

: 1604821-40-0
tert-butyl 5-(2-(3,5-dimethoxybenzamido)thiazol-4-yl)indoline-1-carboxylate

: 1604821-43-3
3,5-dimethoxy-N-(4-(1-(2-methoxyacetyl)-1H-indolin-5-yl)thiazol-2-yl)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: triethylsilane / dichloromethane / 1 h / 20 °C

2: dmap; N-ethyl-N,N-diisopropylamine / dichloromethane / 1 h / 0 - 20 °C

With triethylsilane; dmap; N-ethyl-N,N-diisopropylamine; In dichloromethane;

Reference yield:

: C₁₁H₁₁N₃S

: 1604821-43-3
3,5-dimethoxy-N-(4-(1-(2-methoxyacetyl)-1H-indolin-5-yl)thiazol-2-yl)benzamide

Guidance literature:: Multi-step reaction with 4 steps

1: dmap; N-ethyl-N,N-diisopropylamine / 1 h / 20 °C

2: dmap; N-ethyl-N,N-diisopropylamine / dichloromethane / 1 h / 0 - 20 °C

3: triethylsilane / dichloromethane / 1 h / 20 °C

4: dmap; N-ethyl-N,N-diisopropylamine / dichloromethane / 1 h / 0 - 20 °C

With triethylsilane; dmap; N-ethyl-N,N-diisopropylamine; In dichloromethane;