N-(2-(5-chloro-2-(triethylsilyl)-1H-pyrrolo[2,3-b]pyridin-3-yl)ethyl)-5-(2,5-difluorobenzyl)isoxazole-3-carboxamide

Base Information

Chemical Name:N-(2-(5-chloro-2-(triethylsilyl)-1H-pyrrolo[2,3-b]pyridin-3-yl)ethyl)-5-(2,5-difluorobenzyl)isoxazole-3-carboxamide
CAS No.:1258504-39-0
Molecular Formula:C₂₆H₂₉ClF₂N₄O₂Si
Molecular Weight:531.077
Hs Code.:

Synonyms:N-(2-(5-chloro-2-(triethylsilyl)-1H-pyrrolo[2,3-b]pyridin-3-yl)ethyl)-5-(2,5-difluorobenzyl)isoxazole-3-carboxamide

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Chemical Property of N-(2-(5-chloro-2-(triethylsilyl)-1H-pyrrolo[2,3-b]pyridin-3-yl)ethyl)-5-(2,5-difluorobenzyl)isoxazole-3-carboxamide

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Technology Process of N-(2-(5-chloro-2-(triethylsilyl)-1H-pyrrolo[2,3-b]pyridin-3-yl)ethyl)-5-(2,5-difluorobenzyl)isoxazole-3-carboxamide

There total 7 articles about N-(2-(5-chloro-2-(triethylsilyl)-1H-pyrrolo[2,3-b]pyridin-3-yl)ethyl)-5-(2,5-difluorobenzyl)isoxazole-3-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: 49.0%

: 1258503-80-8
5-(2,5-difluorobenzyl)isoxazole-3-carboxylic acid

: 1258504-38-9
2-(5-chloro-2-(triethylsilyl)-1H-pyrrolo[2,3-b]pyridin-3-yl)ethanamine

: 1258504-39-0
N-(2-(5-chloro-2-(triethylsilyl)-1H-pyrrolo[2,3-b]pyridin-3-yl)ethyl)-5-(2,5-difluorobenzyl)isoxazole-3-carboxamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide; at 20 ℃;

Reference yield:

: 1072-98-6
5-chloro-2-pyridylamine

: 1258504-39-0
N-(2-(5-chloro-2-(triethylsilyl)-1H-pyrrolo[2,3-b]pyridin-3-yl)ethyl)-5-(2,5-difluorobenzyl)isoxazole-3-carboxamide

Guidance literature:: Multi-step reaction with 6 steps

1: iodine; silver sulfate / ethanol / 20 °C

2: sodium carbonate; lithium chloride / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / N,N-dimethyl-formamide / 20 h / 100 °C

3: carbon tetrabromide; triphenylphosphine / tetrahydrofuran / 20 h / 20 °C

4: N,N-dimethyl-formamide / 18 h / 80 °C

5: methanol; triphenylphosphine / 1 h / 80 °C

6: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 20 °C

With methanol; carbon tetrabromide; iodine; sodium carbonate; silver sulfate; N-ethyl-N,N-diisopropylamine; triphenylphosphine; HATU; lithium chloride; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide;

Reference yield:

: 160194-29-6
4-(1,1,1-trimethylsilyl)-3-butyn-1-ol

: 1258504-39-0
N-(2-(5-chloro-2-(triethylsilyl)-1H-pyrrolo[2,3-b]pyridin-3-yl)ethyl)-5-(2,5-difluorobenzyl)isoxazole-3-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1: sodium carbonate; lithium chloride / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / N,N-dimethyl-formamide / 20 h / 100 °C

2: carbon tetrabromide; triphenylphosphine / tetrahydrofuran / 20 h / 20 °C

3: N,N-dimethyl-formamide / 18 h / 80 °C

4: methanol; triphenylphosphine / 1 h / 80 °C

5: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 20 °C

With methanol; carbon tetrabromide; sodium carbonate; N-ethyl-N,N-diisopropylamine; triphenylphosphine; HATU; lithium chloride; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In tetrahydrofuran; N,N-dimethyl-formamide;