(3-chloro-4-(2-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[3,2-c]pyridin-6-ylamino)phenyl)(4-(dimethylamino)piperidin-1-yl)methanone

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Chemical Name:(3-chloro-4-(2-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[3,2-c]pyridin-6-ylamino)phenyl)(4-(dimethylamino)piperidin-1-yl)methanone
CAS No.:1400286-09-0
Molecular Formula:C₂₅H₂₈ClN₇O
Molecular Weight:477.997
Hs Code.:

Synonyms:(3-chloro-4-(2-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[3,2-c]pyridin-6-ylamino)phenyl)(4-(dimethylamino)piperidin-1-yl)methanone

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Chemical Property of (3-chloro-4-(2-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[3,2-c]pyridin-6-ylamino)phenyl)(4-(dimethylamino)piperidin-1-yl)methanone

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Technology Process of (3-chloro-4-(2-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[3,2-c]pyridin-6-ylamino)phenyl)(4-(dimethylamino)piperidin-1-yl)methanone

There total 11 articles about (3-chloro-4-(2-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[3,2-c]pyridin-6-ylamino)phenyl)(4-(dimethylamino)piperidin-1-yl)methanone 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: 97.0%

: 1400285-06-4
tert-butyl 6-(2-chloro-4-(4-(dimethylamino)piperidine-1-carbonyl)phenylamino)-2-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[3,2-c]pyridine-1-carboxylate

: 1400286-09-0
(3-chloro-4-(2-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[3,2-c]pyridin-6-ylamino)phenyl)(4-(dimethylamino)piperidin-1-yl)methanone

Guidance literature:: With trifluoroacetic acid; In dichloromethane; for 2h;
DOI:10.1021/jm401395s

Reference yield:

: 2486-71-7
4-amino-3-chlorobenzoic acid

: 1400286-09-0
(3-chloro-4-(2-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[3,2-c]pyridin-6-ylamino)phenyl)(4-(dimethylamino)piperidin-1-yl)methanone

Guidance literature:: Multi-step reaction with 3 steps

1.1: N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 1 h

1.2: 1 h / 20 °C

2.1: caesium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / 1,4-dioxane; N,N-dimethyl acetamide / 3 h / 80 °C / Inert atmosphere

3.1: trifluoroacetic acid / dichloromethane / 2 h

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; caesium carbonate; N-ethyl-N,N-diisopropylamine; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; trifluoroacetic acid; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In tetrahydrofuran; 1,4-dioxane; dichloromethane; N,N-dimethyl acetamide;
DOI:10.1021/jm401395s

Reference yield:

: 50533-97-6
dimethyl-piperidin-4-yl-amine

: 1400286-09-0
(3-chloro-4-(2-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[3,2-c]pyridin-6-ylamino)phenyl)(4-(dimethylamino)piperidin-1-yl)methanone

Guidance literature:: Multi-step reaction with 3 steps

1.1: N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 1 h

1.2: 1 h / 20 °C

2.1: caesium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / 1,4-dioxane; N,N-dimethyl acetamide / 3 h / 80 °C / Inert atmosphere

3.1: trifluoroacetic acid / dichloromethane / 2 h

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; caesium carbonate; N-ethyl-N,N-diisopropylamine; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; trifluoroacetic acid; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In tetrahydrofuran; 1,4-dioxane; dichloromethane; N,N-dimethyl acetamide;
DOI:10.1021/jm401395s