N-(5-Chloropyridin-2-yl)-5-methyl-2-(4-(N-methylacetimidamido)benzamido)benzamide

Base Information

Chemical Name:N-(5-Chloropyridin-2-yl)-5-methyl-2-(4-(N-methylacetimidamido)benzamido)benzamide
CAS No.:1333126-80-9
Molecular Formula:C₂₃H₂₂ClN₅O₂
Molecular Weight:435.913
Hs Code.:
European Community (EC) Number:844-490-1
ChEMBL ID:CHEMBL5201486

Synonyms:1333126-80-9;CHEMBL5201486;N- (5-Chloropyridin-2-yl)-5-methyl-2-(4-(N-methylacetimidamido)benzamido)benzamide;N-(5-chloropyridin-2-yl)-2-[[4-[ethanimidoyl(methyl)amino]benzoyl]amino]-5-methylbenzamide;SCHEMBL2431134;BDBM50594756;PD121151;EN300-128981;Z1567943550;N-(5-chloropyridin-2-yl)-5-methyl-2-[4-(N-methylethanimidamido)benzamido]benzamide

Suppliers and Price of N-(5-Chloropyridin-2-yl)-5-methyl-2-(4-(N-methylacetimidamido)benzamido)benzamide

Supply Marketing:

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

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Chemical Property of N-(5-Chloropyridin-2-yl)-5-methyl-2-(4-(N-methylacetimidamido)benzamido)benzamide

Chemical Property:

XLogP3:3.8
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:435.1462027
Heavy Atom Count:31
Complexity:652

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC(=C(C=C1)NC(=O)C2=CC=C(C=C2)N(C)C(=N)C)C(=O)NC3=NC=C(C=C3)Cl

Technology Process of N-(5-Chloropyridin-2-yl)-5-methyl-2-(4-(N-methylacetimidamido)benzamido)benzamide

There total 8 articles about N-(5-Chloropyridin-2-yl)-5-methyl-2-(4-(N-methylacetimidamido)benzamido)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:

: 1333127-02-8
N-(5-chloropyridine-2-yl)-2-[(4-methylaminophenylcarbonyl)amino]-5-methylbenzamide

: 75-05-8,26809-02-9
acetonitrile

: 1333126-80-9
N-(5-chloropyridine-2-yl)-2-[(4-etanimidoil(methyl)aminophenylcarbonyl)amino]-5-methylbenzamide

Guidance literature:: Heating; Cooling with ice;

Reference yield:

: 280773-04-8
N-(5-chloro(pyridin-2-yl))(5-methyl-2-nitrophenyl)carboxamide

: 1333126-80-9
N-(5-chloropyridine-2-yl)-2-[(4-etanimidoil(methyl)aminophenylcarbonyl)amino]-5-methylbenzamide

Guidance literature:: Multi-step reaction with 4 steps

1: tin(ll) chloride; hydrogenchloride / ethyl acetate; water / 4 h / Heating

2: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / tetrahydrofuran / 72 h

3: sodium hydroxide / isopropyl alcohol / 3 h

4: Heating; Cooling with ice

With hydrogenchloride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; tin(ll) chloride; sodium hydroxide; In tetrahydrofuran; water; ethyl acetate; isopropyl alcohol;

Reference yield:

: 280773-05-9
N-(5-chloropyridin-2-yl)-2-amino-5-methylbenzamide

: 1333126-80-9
N-(5-chloropyridine-2-yl)-2-[(4-etanimidoil(methyl)aminophenylcarbonyl)amino]-5-methylbenzamide

Guidance literature:: Multi-step reaction with 3 steps

1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / tetrahydrofuran / 72 h

2: sodium hydroxide / isopropyl alcohol / 3 h

3: Heating; Cooling with ice

With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; sodium hydroxide; In tetrahydrofuran; isopropyl alcohol;