1-[3-(2-methoxy-4-trifluoromethyl-benzoylamino)-propyl]-1H-[1,2,3]triazole-4-carboxylic acid [cyano-(4-ethyl-phenyl)-methyl]-amide

Base Information

Chemical Name:1-[3-(2-methoxy-4-trifluoromethyl-benzoylamino)-propyl]-1H-[1,2,3]triazole-4-carboxylic acid [cyano-(4-ethyl-phenyl)-methyl]-amide
CAS No.:1613253-46-5
Molecular Formula:C₂₅H₂₅F₃N₆O₃
Molecular Weight:514.507
Hs Code.:

Synonyms:1-[3-(2-methoxy-4-trifluoromethyl-benzoylamino)-propyl]-1H-[1,2,3]triazole-4-carboxylic acid [cyano-(4-ethyl-phenyl)-methyl]-amide

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Chemical Property of 1-[3-(2-methoxy-4-trifluoromethyl-benzoylamino)-propyl]-1H-[1,2,3]triazole-4-carboxylic acid [cyano-(4-ethyl-phenyl)-methyl]-amide

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Technology Process of 1-[3-(2-methoxy-4-trifluoromethyl-benzoylamino)-propyl]-1H-[1,2,3]triazole-4-carboxylic acid [cyano-(4-ethyl-phenyl)-methyl]-amide

There total 4 articles about 1-[3-(2-methoxy-4-trifluoromethyl-benzoylamino)-propyl]-1H-[1,2,3]triazole-4-carboxylic acid [cyano-(4-ethyl-phenyl)-methyl]-amide 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: 66.0%

: 1613253-80-7
1-[3-(2-methoxy-4-trifluoromethyl-benzoylamino)-propyl]-1H-[1,2,3] triazole-4-carboxylic acid

: 2-amino-2-(4-ethylphenyl)acetonitrile hydrochloride

: 1613253-46-5
1-[3-(2-methoxy-4-trifluoromethyl-benzoylamino)-propyl]-1H-[1,2,3]triazole-4-carboxylic acid [cyano-(4-ethyl-phenyl)-methyl]-amide

Guidance literature:: 1-[3-(2-methoxy-4-trifluoromethyl-benzoylamino)-propyl]-1H-[1,2,3] triazole-4-carboxylic acid; With N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl acetamide; at 0 ℃; for 0.75h;

2-amino-2-(4-ethylphenyl)acetonitrile hydrochloride; In N,N-dimethyl acetamide; at 20 ℃;

Reference yield:

: 1613253-79-4
1-[3-(2-methoxy-4-trifluoromethyl-benzoylamino)-propyl]-1H-[1,2,3]triazole-4-carboxylic acid methyl ester

: 1613253-46-5
1-[3-(2-methoxy-4-trifluoromethyl-benzoylamino)-propyl]-1H-[1,2,3]triazole-4-carboxylic acid [cyano-(4-ethyl-phenyl)-methyl]-amide

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium hydroxide; water / methanol / 20 °C

2.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl acetamide / 0.75 h / 0 °C

2.2: 20 °C

With water; N-ethyl-N,N-diisopropylamine; HATU; sodium hydroxide; In methanol; N,N-dimethyl acetamide;

Reference yield:

: 1613253-77-2
1-(3-tert-butoxycarbonylamino-propyl)-1H-[1,2,3]triazole-4-carboxylic acid methyl ester

: 1613253-46-5
1-[3-(2-methoxy-4-trifluoromethyl-benzoylamino)-propyl]-1H-[1,2,3]triazole-4-carboxylic acid [cyano-(4-ethyl-phenyl)-methyl]-amide

Guidance literature:: Multi-step reaction with 4 steps

1.1: hydrogenchloride / 1,4-dioxane / 20 °C

2.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl acetamide / 1 h / 0 °C / Cooling with ice

2.2: 20 °C

3.1: sodium hydroxide; water / methanol / 20 °C

4.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl acetamide / 0.75 h / 0 °C

4.2: 20 °C

With hydrogenchloride; water; N-ethyl-N,N-diisopropylamine; HATU; sodium hydroxide; In 1,4-dioxane; methanol; N,N-dimethyl acetamide;