5-anilino-3-{[4-(4-methylpiperazin-1-yl)phenyl]amino}pyridine-2-carboxamide

Base Information

Chemical Name:5-anilino-3-{[4-(4-methylpiperazin-1-yl)phenyl]amino}pyridine-2-carboxamide
CAS No.:1389440-98-5
Molecular Formula:C₂₃H₂₆N₆O
Molecular Weight:402.499
Hs Code.:

Synonyms:5-anilino-3-{[4-(4-methylpiperazin-1-yl)phenyl]amino}pyridine-2-carboxamide

Suppliers and Price of 5-anilino-3-{[4-(4-methylpiperazin-1-yl)phenyl]amino}pyridine-2-carboxamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 5-anilino-3-{[4-(4-methylpiperazin-1-yl)phenyl]amino}pyridine-2-carboxamide

Chemical Property:

Purity/Quality:: 99% ^*data from raw suppliers

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Technology Process of 5-anilino-3-{[4-(4-methylpiperazin-1-yl)phenyl]amino}pyridine-2-carboxamide

There total 3 articles about 5-anilino-3-{[4-(4-methylpiperazin-1-yl)phenyl]amino}pyridine-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:

: 1389441-00-2
3-[4-(4-methyl-piperazin-1-yl)-phenylamino]-5-phenylamino-pyridine-2-carbonitrile

: 1389440-98-5
5-anilino-3-{[4-(4-methylpiperazin-1-yl)phenyl]amino}pyridine-2-carboxamide

Guidance literature:: 3-[4-(4-methyl-piperazin-1-yl)-phenylamino]-5-phenylamino-pyridine-2-carbonitrile; With dihydrogen peroxide; potassium carbonate; In dimethyl sulfoxide; at 0 - 20 ℃; for 19h;

With water; In dimethyl sulfoxide;

Reference yield:

: 573675-25-9
5-bromo-3-nitropyridine-2-carbonitrile

: 1389440-98-5
5-anilino-3-{[4-(4-methylpiperazin-1-yl)phenyl]amino}pyridine-2-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1: tetrabutyl ammonium fluoride / tetrahydrofuran / 1 h / -25 - 20 °C

2: triethylamine / isopropyl alcohol / Microwave irradiation

3: caesium carbonate / palladium diacetate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl / toluene / 3 h / 110 °C / Microwave irradiation; Inert atmosphere

4: potassium carbonate; dihydrogen peroxide / dimethyl sulfoxide / 19 h / 0 - 20 °C

With tetrabutyl ammonium fluoride; dihydrogen peroxide; potassium carbonate; caesium carbonate; triethylamine; palladium diacetate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; In tetrahydrofuran; dimethyl sulfoxide; isopropyl alcohol; toluene;

Reference yield:

: 886373-28-0
5-bromo-3-fluoropyridine-2-carbonitrile

: 1389440-98-5
5-anilino-3-{[4-(4-methylpiperazin-1-yl)phenyl]amino}pyridine-2-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / isopropyl alcohol / Microwave irradiation

2: caesium carbonate / palladium diacetate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl / toluene / 3 h / 110 °C / Microwave irradiation; Inert atmosphere

3: potassium carbonate; dihydrogen peroxide / dimethyl sulfoxide / 19 h / 0 - 20 °C

With dihydrogen peroxide; potassium carbonate; caesium carbonate; triethylamine; palladium diacetate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; In dimethyl sulfoxide; isopropyl alcohol; toluene;