ethyl 2-ethylthio-3-[4-methoxy-3-[N-[[4-(trifluoromethyl)phenyl]methyl]carbamoyl]phenyl]propanoate

Base Information

Chemical Name:ethyl 2-ethylthio-3-[4-methoxy-3-[N-[[4-(trifluoromethyl)phenyl]methyl]carbamoyl]phenyl]propanoate
CAS No.:311770-79-3
Molecular Formula:C₂₃H₂₆F₃NO₄S
Molecular Weight:469.525
Hs Code.:

Synonyms:ethyl 2-ethylthio-3-[4-methoxy-3-[N-[[4-(trifluoromethyl)phenyl]methyl]carbamoyl]phenyl]propanoate

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Chemical Property of ethyl 2-ethylthio-3-[4-methoxy-3-[N-[[4-(trifluoromethyl)phenyl]methyl]carbamoyl]phenyl]propanoate

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Technology Process of ethyl 2-ethylthio-3-[4-methoxy-3-[N-[[4-(trifluoromethyl)phenyl]methyl]carbamoyl]phenyl]propanoate

There total 6 articles about ethyl 2-ethylthio-3-[4-methoxy-3-[N-[[4-(trifluoromethyl)phenyl]methyl]carbamoyl]phenyl]propanoate 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: 43.0%

: 311770-78-2
ethyl 2-bromo-3-[4-methoxy-3-[N-[[4-(trifluoromethyl)phenyl]methyl]carbamoyl]phenyl]propanoate

: 811-51-8
sodium thioethylate

: 311770-79-3
ethyl 2-ethylthio-3-[4-methoxy-3-[N-[[4-(trifluoromethyl)phenyl]methyl]carbamoyl]phenyl]propanoate

Guidance literature:: In ethanol; for 1.5h; Heating;
DOI:10.1021/jm0205144

Reference yield:

: 40751-89-1
2-methoxy-5-nitrobenzoic acid

: 311770-79-3
ethyl 2-ethylthio-3-[4-methoxy-3-[N-[[4-(trifluoromethyl)phenyl]methyl]carbamoyl]phenyl]propanoate

Guidance literature:: Multi-step reaction with 5 steps

1.1: Et₃N / CH₂Cl₂ / -10 °C

2.1: CH₂Cl₂ / -10 - 20 °C

3.1: H₂ / Pd/C / tetrahydrofuran; ethanol / 2207.43 Torr

4.1: aq. HBr; NaNO₂ / acetone; methanol / 0.17 h / 0 °C

4.2: 71 percent / CuO / acetone; methanol / 0.5 h / 20 °C

5.1: 43 percent / ethanol / 1.5 h / Heating

With hydrogen bromide; hydrogen; triethylamine; sodium nitrite; palladium on activated charcoal; In tetrahydrofuran; methanol; ethanol; dichloromethane; acetone;
DOI:10.1021/jm0205144

Reference yield:

: 3300-51-4
p-Trifluoromethylbenzylamine

: 311770-79-3
ethyl 2-ethylthio-3-[4-methoxy-3-[N-[[4-(trifluoromethyl)phenyl]methyl]carbamoyl]phenyl]propanoate

Guidance literature:: Multi-step reaction with 4 steps

1.1: CH₂Cl₂ / -10 - 20 °C

2.1: H₂ / Pd/C / tetrahydrofuran; ethanol / 2207.43 Torr

3.1: aq. HBr; NaNO₂ / acetone; methanol / 0.17 h / 0 °C

3.2: 71 percent / CuO / acetone; methanol / 0.5 h / 20 °C

4.1: 43 percent / ethanol / 1.5 h / Heating

With hydrogen bromide; hydrogen; sodium nitrite; palladium on activated charcoal; In tetrahydrofuran; methanol; ethanol; dichloromethane; acetone;
DOI:10.1021/jm0205144