methyl 2-methyl-5-[(E)-3-oxo-3-[[2,2,2-trifluoro-1-[3-(trifluoromethyl)phenyl]ethyl]amino]prop-1-enyl]thiophene-3-carboxylate

Base Information

Chemical Name:methyl 2-methyl-5-[(E)-3-oxo-3-[[2,2,2-trifluoro-1-[3-(trifluoromethyl)phenyl]ethyl]amino]prop-1-enyl]thiophene-3-carboxylate
CAS No.:1467070-89-8
Molecular Formula:C₁₉H₁₅F₆NO₃S
Molecular Weight:451.389
Hs Code.:

Synonyms:methyl 2-methyl-5-[(E)-3-oxo-3-[[2,2,2-trifluoro-1-[3-(trifluoromethyl)phenyl]ethyl]amino]prop-1-enyl]thiophene-3-carboxylate

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Chemical Property of methyl 2-methyl-5-[(E)-3-oxo-3-[[2,2,2-trifluoro-1-[3-(trifluoromethyl)phenyl]ethyl]amino]prop-1-enyl]thiophene-3-carboxylate

Chemical Property:

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Technology Process of methyl 2-methyl-5-[(E)-3-oxo-3-[[2,2,2-trifluoro-1-[3-(trifluoromethyl)phenyl]ethyl]amino]prop-1-enyl]thiophene-3-carboxylate

There total 3 articles about methyl 2-methyl-5-[(E)-3-oxo-3-[[2,2,2-trifluoro-1-[3-(trifluoromethyl)phenyl]ethyl]amino]prop-1-enyl]thiophene-3-carboxylate 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:

: 65686-68-2,1213368-14-9,1213841-80-5
2,2,2-trifluoro-1-[3-(trifluoromethyl)phenyl]ethanamine

: 1467070-86-5
(E)-3-(4-methoxycarbonyl-5-methyl-2-thienyl)prop-2-enoic acid

: 1467070-89-8
methyl 2-methyl-5-[(E)-3-oxo-3-[[2,2,2-trifluoro-1-[3-(trifluoromethyl)phenyl]ethyl]amino]prop-1-enyl]thiophene-3-carboxylate

Guidance literature:: With HATU; In tetrahydrofuran; at 20 ℃;

Reference yield:

: 1467070-87-6
methyl 5-[(E)-3-tert-butoxy-3-oxoprop-1-enyl]-2-methylthiophene-3-carboxylate

: 1467070-89-8
methyl 2-methyl-5-[(E)-3-oxo-3-[[2,2,2-trifluoro-1-[3-(trifluoromethyl)phenyl]ethyl]amino]prop-1-enyl]thiophene-3-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogenchloride / ethyl acetate / 20 °C

2: HATU / tetrahydrofuran / 20 °C

With hydrogenchloride; HATU; In tetrahydrofuran; ethyl acetate;

Reference yield:

: 1259396-11-6
methyl 5-bromo-2-methylthiophene-3-carboxylate

: 1467070-89-8
methyl 2-methyl-5-[(E)-3-oxo-3-[[2,2,2-trifluoro-1-[3-(trifluoromethyl)phenyl]ethyl]amino]prop-1-enyl]thiophene-3-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: tris-(o-tolyl)phosphine; palladium diacetate; triethylamine / N,N-dimethyl-formamide / Inert atmosphere; Reflux

2: hydrogenchloride / ethyl acetate / 20 °C

3: HATU / tetrahydrofuran / 20 °C

With hydrogenchloride; palladium diacetate; triethylamine; HATU; tris-(o-tolyl)phosphine; In tetrahydrofuran; ethyl acetate; N,N-dimethyl-formamide;