N-[4-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-a]pyridin-6-yl}oxy)phenyl]-3-methyl-1-phenyl-1H-pyrazole-5-carboxamide

Base Information

Chemical Name:N-[4-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-a]pyridin-6-yl}oxy)phenyl]-3-methyl-1-phenyl-1H-pyrazole-5-carboxamide
CAS No.:1195778-60-9
Molecular Formula:C₂₈H₂₄N₆O₃
Molecular Weight:492.537
Hs Code.:

Synonyms:N-[4-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-a]pyridin-6-yl}oxy)phenyl]-3-methyl-1-phenyl-1H-pyrazole-5-carboxamide

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Chemical Property of N-[4-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-a]pyridin-6-yl}oxy)phenyl]-3-methyl-1-phenyl-1H-pyrazole-5-carboxamide

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Technology Process of N-[4-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-a]pyridin-6-yl}oxy)phenyl]-3-methyl-1-phenyl-1H-pyrazole-5-carboxamide

There total 9 articles about N-[4-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-a]pyridin-6-yl}oxy)phenyl]-3-methyl-1-phenyl-1H-pyrazole-5-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: 29.0%

: 1136-76-1
3-methyl-1-phenyl-1H-pyrazole-5-carboxylic acid

: 1195781-14-6
N-[6-(4-aminophenoxy)imidazo[1,2-a]pyridin-2-yl]cyclopropanecarboxamide

: 1195778-60-9
N-[4-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-a]pyridin-6-yl}oxy)phenyl]-3-methyl-1-phenyl-1H-pyrazole-5-carboxamide

Guidance literature:: 3-methyl-1-phenyl-1H-pyrazole-5-carboxylic acid; With oxalyl dichloride; N,N-dimethyl-formamide; In N,N-dimethyl-formamide; at 20 ℃; Cooling with ice;

N-[6-(4-aminophenoxy)imidazo[1,2-a]pyridin-2-yl]cyclopropanecarboxamide; In ISOPROPYLAMIDE; N,N-dimethyl-formamide; at 20 ℃; for 2h;

With sodium hydrogencarbonate; In ISOPROPYLAMIDE; water; N,N-dimethyl-formamide;

Reference yield:

: 1195781-09-9
benzyl {4-[(6-{[(4-methylphenyl)sulfonyl]amino}pyridin-3-yl)oxy]phenyl}carbamate

: 1195778-60-9
N-[4-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-a]pyridin-6-yl}oxy)phenyl]-3-methyl-1-phenyl-1H-pyrazole-5-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 24 h / 20 °C

2.1: trifluoroacetic anhydride / tetrahydrofuran / 48 h / 20 °C

2.3: 10 h / 45 °C

3.1: ISOPROPYLAMIDE / 1 h / 20 °C

4.1: water; barium(II) hydroxide / 1,2-dimethoxyethane / 36 h / 90 °C

5.1: oxalyl dichloride / N,N-dimethyl-formamide / N,N-dimethyl-formamide / 20 °C / Cooling with ice

5.2: 2 h / 20 °C

With oxalyl dichloride; water; N-ethyl-N,N-diisopropylamine; trifluoroacetic anhydride; barium(II) hydroxide; N,N-dimethyl-formamide; In tetrahydrofuran; 1,2-dimethoxyethane; ISOPROPYLAMIDE; N,N-dimethyl-formamide;

Reference yield:

: 1195781-07-7
benzyl {4-[(6-aminopyridin-3-yl)oxy]phenyl}carbamate

: 1195778-60-9
N-[4-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-a]pyridin-6-yl}oxy)phenyl]-3-methyl-1-phenyl-1H-pyrazole-5-carboxamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: pyridine / 16 h / 20 °C

2.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 24 h / 20 °C

3.1: trifluoroacetic anhydride / tetrahydrofuran / 48 h / 20 °C

3.3: 10 h / 45 °C

4.1: ISOPROPYLAMIDE / 1 h / 20 °C

5.1: water; barium(II) hydroxide / 1,2-dimethoxyethane / 36 h / 90 °C

6.1: oxalyl dichloride / N,N-dimethyl-formamide / N,N-dimethyl-formamide / 20 °C / Cooling with ice

6.2: 2 h / 20 °C

With pyridine; oxalyl dichloride; water; N-ethyl-N,N-diisopropylamine; trifluoroacetic anhydride; barium(II) hydroxide; N,N-dimethyl-formamide; In tetrahydrofuran; 1,2-dimethoxyethane; ISOPROPYLAMIDE; N,N-dimethyl-formamide;