N-(4-(5-amino-1-(4-methoxybenzyl)-1H-pyrazol-4-ylcarbamoyl)-3-methylphenyl)-5-methylisoxazole-3-carboxamide

Base Information

Chemical Name:N-(4-(5-amino-1-(4-methoxybenzyl)-1H-pyrazol-4-ylcarbamoyl)-3-methylphenyl)-5-methylisoxazole-3-carboxamide
CAS No.:1292281-85-6
Molecular Formula:C₂₄H₂₄N₆O₄
Molecular Weight:460.492
Hs Code.:

Synonyms:N-(4-(5-amino-1-(4-methoxybenzyl)-1H-pyrazol-4-ylcarbamoyl)-3-methylphenyl)-5-methylisoxazole-3-carboxamide

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Chemical Property of N-(4-(5-amino-1-(4-methoxybenzyl)-1H-pyrazol-4-ylcarbamoyl)-3-methylphenyl)-5-methylisoxazole-3-carboxamide

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Technology Process of N-(4-(5-amino-1-(4-methoxybenzyl)-1H-pyrazol-4-ylcarbamoyl)-3-methylphenyl)-5-methylisoxazole-3-carboxamide

There total 5 articles about N-(4-(5-amino-1-(4-methoxybenzyl)-1H-pyrazol-4-ylcarbamoyl)-3-methylphenyl)-5-methylisoxazole-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:

: 3405-77-4
5-methylisoxazole 3-carboxylic acid

: 1292281-67-4
N-(5-amino-1-(4-methoxybenzyl)-1H-pyrazol-4-yl)-2-methyl-4-aminobenzamide

: 1292281-85-6
N-(4-(5-amino-1-(4-methoxybenzyl)-1H-pyrazol-4-ylcarbamoyl)-3-methylphenyl)-5-methylisoxazole-3-carboxamide

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1016/j.bmc.2011.01.067

Reference yield:

: 1236202-77-9
1-(4-methoxybenzyl)-4-nitroso-1H-pyrazol-5-amine

: 1292281-85-6
N-(4-(5-amino-1-(4-methoxybenzyl)-1H-pyrazol-4-ylcarbamoyl)-3-methylphenyl)-5-methylisoxazole-3-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: hydrogenchloride; tin(II) chloride dihdyrate / ethanol; water / 0.75 h / 80 °C

1.2: pH 7 - 8 / Cooling with ice

2.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / N,N-dimethyl-formamide / 4 h / 80 °C

3.1: hydrogenchloride; tin(II) chloride dihdyrate / ethanol / 1.5 h / 80 °C

4.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / N,N-dimethyl-formamide / 20 °C

With hydrogenchloride; tin(II) chloride dihdyrate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In ethanol; water; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2011.01.067

Reference yield:

: 4,5-diamino-1-(4'-methoxybenzyl)-1H-pyrazole

: 1292281-85-6
N-(4-(5-amino-1-(4-methoxybenzyl)-1H-pyrazol-4-ylcarbamoyl)-3-methylphenyl)-5-methylisoxazole-3-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / N,N-dimethyl-formamide / 4 h / 80 °C

2: hydrogenchloride; tin(II) chloride dihdyrate / ethanol / 1.5 h / 80 °C

3: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / N,N-dimethyl-formamide / 20 °C

With hydrogenchloride; tin(II) chloride dihdyrate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In ethanol; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2011.01.067