1-{4-[5-(3,4,5-trichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]phenyl}azetidine-3-carboxylic acid-(2,2,2-trifluoro-ethyl)amide

Base Information

Chemical Name:1-{4-[5-(3,4,5-trichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]phenyl}azetidine-3-carboxylic acid-(2,2,2-trifluoro-ethyl)amide
CAS No.:1401102-78-0
Molecular Formula:C₂₂H₁₆Cl₃F₆N₃O₂
Molecular Weight:574.737
Hs Code.:

Synonyms:1-{4-[5-(3,4,5-trichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]phenyl}azetidine-3-carboxylic acid-(2,2,2-trifluoro-ethyl)amide

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Chemical Property of 1-{4-[5-(3,4,5-trichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]phenyl}azetidine-3-carboxylic acid-(2,2,2-trifluoro-ethyl)amide

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Technology Process of 1-{4-[5-(3,4,5-trichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]phenyl}azetidine-3-carboxylic acid-(2,2,2-trifluoro-ethyl)amide

There total 4 articles about 1-{4-[5-(3,4,5-trichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]phenyl}azetidine-3-carboxylic acid-(2,2,2-trifluoro-ethyl)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: 71.0%

: 1401102-96-2
1-{4-[5-(3,4,5-trichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]phenyl}azetidine-3-carboxylic acid

: 373-88-6
2,2,2-trifluroethylamine hydrochloride

: 1401102-78-0
1-{4-[5-(3,4,5-trichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]phenyl}azetidine-3-carboxylic acid-(2,2,2-trifluoro-ethyl)amide

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 0 - 20 ℃; for 16h; Inert atmosphere;

Reference yield:

: 1401102-95-1
1-{4-[5-(3,4,5-trichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]phenyl}azetidine-3-carboxylic acid methyl ester

: 1401102-78-0
1-{4-[5-(3,4,5-trichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]phenyl}azetidine-3-carboxylic acid-(2,2,2-trifluoro-ethyl)amide

Guidance literature:: Multi-step reaction with 2 steps

1.1: water; lithium hydroxide / tetrahydrofuran; methanol / 24 h / 20 °C

1.2: pH ~ 4

2.1: N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 16 h / 0 - 20 °C / Inert atmosphere

With water; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; lithium hydroxide; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;

Reference yield:

: 1401102-94-0
1-[4-(hydroxyiminomethyl)phenyl]azetidine-3-carboxylic acid methyl ester

: 1401102-78-0
1-{4-[5-(3,4,5-trichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]phenyl}azetidine-3-carboxylic acid-(2,2,2-trifluoro-ethyl)amide

Guidance literature:: Multi-step reaction with 3 steps

1.1: N-chloro-succinimide / N,N-dimethyl-formamide / 2 h / 0 - 10 °C

1.2: 4 h / 20 °C / Inert atmosphere

2.1: water; lithium hydroxide / tetrahydrofuran; methanol / 24 h / 20 °C

2.2: pH ~ 4

3.1: N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 16 h / 0 - 20 °C / Inert atmosphere

With N-chloro-succinimide; water; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; lithium hydroxide; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;