(Z)-N-(3-(azetidin-3-ylmethyl)-5-tert-butylthiazol-2(3H)-ylidene)-2-methoxy-5-(trifluoromethyl)benzamide

Base Information

Chemical Name:(Z)-N-(3-(azetidin-3-ylmethyl)-5-tert-butylthiazol-2(3H)-ylidene)-2-methoxy-5-(trifluoromethyl)benzamide
CAS No.:1065640-11-0
Molecular Formula:C₂₀H₂₄F₃N₃O₂S
Molecular Weight:427.491
Hs Code.:

Synonyms:(Z)-N-(3-(azetidin-3-ylmethyl)-5-tert-butylthiazol-2(3H)-ylidene)-2-methoxy-5-(trifluoromethyl)benzamide

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Chemical Property of (Z)-N-(3-(azetidin-3-ylmethyl)-5-tert-butylthiazol-2(3H)-ylidene)-2-methoxy-5-(trifluoromethyl)benzamide

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Technology Process of (Z)-N-(3-(azetidin-3-ylmethyl)-5-tert-butylthiazol-2(3H)-ylidene)-2-methoxy-5-(trifluoromethyl)benzamide

There total 4 articles about (Z)-N-(3-(azetidin-3-ylmethyl)-5-tert-butylthiazol-2(3H)-ylidene)-2-methoxy-5-(trifluoromethyl)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:

: 2987-16-8
3,3-dimethylbutyrylaldehyde

: 1065640-11-0
(Z)-N-(3-(azetidin-3-ylmethyl)-5-tert-butylthiazol-2(3H)-ylidene)-2-methoxy-5-(trifluoromethyl)benzamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: acetonitrile / 72 h / 20 °C / Molecular sieve

1.2: 50 °C

2.1: triethylamine / tetrahydrofuran / 76 h / 20 - 50 °C

3.1: trifluoroacetic acid / dichloromethane / 0 - 20 °C

With triethylamine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; acetonitrile;

Reference yield:

: 1065640-09-6
tert-butyl 3-((5-tert-butyl-2-iminothiazol-3(2H)-yl)methyl)azetidine-1-carboxylate

: 1065640-11-0
(Z)-N-(3-(azetidin-3-ylmethyl)-5-tert-butylthiazol-2(3H)-ylidene)-2-methoxy-5-(trifluoromethyl)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / tetrahydrofuran / 76 h / 20 - 50 °C

2: trifluoroacetic acid / dichloromethane / 0 - 20 °C

With triethylamine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane;

Reference yield:

: 4864-01-1
2-methoxy-5-(trifluoromethyl)-benzoic acid

: 1065640-11-0
(Z)-N-(3-(azetidin-3-ylmethyl)-5-tert-butylthiazol-2(3H)-ylidene)-2-methoxy-5-(trifluoromethyl)benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: thionyl chloride / toluene / 2 h / Reflux

2: triethylamine / tetrahydrofuran / 76 h / 20 - 50 °C

3: trifluoroacetic acid / dichloromethane / 0 - 20 °C

With thionyl chloride; triethylamine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; toluene;