methyl (2E)-3-(4-{[2-{isobutyl[(5-methyl-2-furyl)sulfonyl]amino}-5-(trifluoromethyl)phenoxy]methyl}phenyl)acrylate

Base Information

Chemical Name:methyl (2E)-3-(4-{[2-{isobutyl[(5-methyl-2-furyl)sulfonyl]amino}-5-(trifluoromethyl)phenoxy]methyl}phenyl)acrylate
CAS No.:913078-92-9
Molecular Formula:C₂₇H₂₈F₃NO₆S
Molecular Weight:551.584
Hs Code.:

Synonyms:methyl (2E)-3-(4-{[2-{isobutyl[(5-methyl-2-furyl)sulfonyl]amino}-5-(trifluoromethyl)phenoxy]methyl}phenyl)acrylate

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Chemical Property of methyl (2E)-3-(4-{[2-{isobutyl[(5-methyl-2-furyl)sulfonyl]amino}-5-(trifluoromethyl)phenoxy]methyl}phenyl)acrylate

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Technology Process of methyl (2E)-3-(4-{[2-{isobutyl[(5-methyl-2-furyl)sulfonyl]amino}-5-(trifluoromethyl)phenoxy]methyl}phenyl)acrylate

There total 12 articles about methyl (2E)-3-(4-{[2-{isobutyl[(5-methyl-2-furyl)sulfonyl]amino}-5-(trifluoromethyl)phenoxy]methyl}phenyl)acrylate 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: 94.0%

: 913078-89-4
methyl (2E)-3-(4-{[2-{[(5-methyl-2-furyl)sulfonyl]amino}-5-(trifluoromethyl)phenoxy]methyl}phenyl)acrylate

: 513-38-2
Isobutyl iodide

: 913078-92-9
methyl (2E)-3-(4-{[2-{isobutyl[(5-methyl-2-furyl)sulfonyl]amino}-5-(trifluoromethyl)phenoxy]methyl}phenyl)acrylate

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 80 ℃;
DOI:10.1016/j.bmc.2006.06.067

Reference yield:

: 534-22-5
2-methylfuran

: 913078-92-9
methyl (2E)-3-(4-{[2-{isobutyl[(5-methyl-2-furyl)sulfonyl]amino}-5-(trifluoromethyl)phenoxy]methyl}phenyl)acrylate

Guidance literature:: Multi-step reaction with 4 steps

1: 93 percent / acetonitrile / 23 h / 40 °C

2: 41 percent / oxalyl chloride / 1,2-dimethoxy-ethane; dimethylformamide / 3 h / 20 °C

3: 80 percent / pyridine / CH₂Cl₂ / 9 h

4: 94 percent / potassium carbonate / dimethylformamide / 80 °C

With pyridine; oxalyl dichloride; potassium carbonate; In 1,2-dimethoxyethane; dichloromethane; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1016/j.bmc.2006.06.067

Reference yield:

: 907587-46-6
methyl 4-[(2-nitro-5-(trifluoromethyl)phenoxy)methyl]benzoate

: 913078-92-9
methyl (2E)-3-(4-{[2-{isobutyl[(5-methyl-2-furyl)sulfonyl]amino}-5-(trifluoromethyl)phenoxy]methyl}phenyl)acrylate

Guidance literature:: Multi-step reaction with 7 steps

1: 85 percent / lithium borohydride / diethyl ether; methanol / Heating

2: 81 percent / dimethylsulfoxide; sulfur trioxide pyridine complex; diisopropylethylamine / ethyl acetate / 0.5 h

3: 90 percent / piperidine; pyridine / 0.5 h / 100 °C

4: 100 percent / potassium carbonate / dimethylformamide / 1.5 h / 65 °C

5: 91 percent / iron; acetic acid / H₂O / 0.5 h / 50 °C

6: 80 percent / pyridine / CH₂Cl₂ / 9 h

7: 94 percent / potassium carbonate / dimethylformamide / 80 °C

With piperidine; pyridine; lithium borohydride; sulfur trioxide pyridine complex; iron; potassium carbonate; acetic acid; dimethyl sulfoxide; N-ethyl-N,N-diisopropylamine; In methanol; diethyl ether; dichloromethane; water; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2006.06.067