(E)-((N'-(4-methoxy-2-methylphenyl)-N-((4-(1-(4-(trifluoromethyl)phenyl)-1H-1,2,4-triazol-3-yl)phenyl)carbamoyl)carbamimidoyl)thio)methyl isobutyrate

Base Information

Chemical Name:(E)-((N'-(4-methoxy-2-methylphenyl)-N-((4-(1-(4-(trifluoromethyl)phenyl)-1H-1,2,4-triazol-3-yl)phenyl)carbamoyl)carbamimidoyl)thio)methyl isobutyrate
CAS No.:1417911-05-7
Molecular Formula:C₃₀H₂₉F₃N₆O₄S
Molecular Weight:626.659
Hs Code.:

(E)-((N'-(4-methoxy-2-methylphenyl)-N-((4-(1-(4-(trifluoromethyl)phenyl)-1H-1,2,4-triazol-3-yl)phenyl)carbamoyl)carbamimidoyl)thio)methyl isobutyrate

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Chemical Property of (E)-((N'-(4-methoxy-2-methylphenyl)-N-((4-(1-(4-(trifluoromethyl)phenyl)-1H-1,2,4-triazol-3-yl)phenyl)carbamoyl)carbamimidoyl)thio)methyl isobutyrate

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Technology Process of (E)-((N'-(4-methoxy-2-methylphenyl)-N-((4-(1-(4-(trifluoromethyl)phenyl)-1H-1,2,4-triazol-3-yl)phenyl)carbamoyl)carbamimidoyl)thio)methyl isobutyrate

There total 4 articles about (E)-((N'-(4-methoxy-2-methylphenyl)-N-((4-(1-(4-(trifluoromethyl)phenyl)-1H-1,2,4-triazol-3-yl)phenyl)carbamoyl)carbamimidoyl)thio)methyl isobutyrate 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: 61.0%

: 1417885-49-4
4-nitrophenyl 4-(1-(4-(trifluoromethyl)phenyl)-1H-1,2,4-triazol-3-yl)phenylcarbamate

: 1417885-48-3
(E)-(N-(4-methoxy-2-methylphenyl)carbamimidoylthio)methyl isobutyrate hydrobromide

: 1417911-05-7,1421843-97-1
(E)-((N'-(4-methoxy-2-methylphenyl)N-((4-(1-(4-(trifluoromethyl)phenyl)-1H-1,2,4-triazol-3-yl)phenyl)carbamoyl)carbamimidoyl)thio)methyl isobutyrate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at 20 ℃; for 2h;

Reference yield: 61.0%

: 1417885-49-4
4-nitrophenyl 4-(1-(4-(trifluoromethyl)phenyl)-1H-1,2,4-triazol-3-yl)phenylcarbamate

: 1417885-48-3
(E)-(N'-(4-methoxy-2-methylphenyl)carbamimidoylthio)methyl isobutyrate hydrobromide

: 1417911-05-7,1421843-97-1
(E)-((N'-(4-methoxy-2-methylphenyl)-N-((4-(1-(4-(trifluoromethyl)phenyl)-1H-1,2,4-triazol-3-yl)phenyl)carbamoyl)carbamimidoyl)thio)methyl isobutyrate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at 20 ℃; for 2h;

Reference yield:

: 1-(4-methoxy-2-methylphenyl)thiourea

: 74416-82-3
bromomethyl isobutyrate

: 1417911-05-7,1421843-97-1
(E)-((N'-(4-methoxy-2-methylphenyl)N-((4-(1-(4-(trifluoromethyl)phenyl)-1H-1,2,4-triazol-3-yl)phenyl)carbamoyl)carbamimidoyl)thio)methyl isobutyrate

Guidance literature:: Multi-step reaction with 2 steps

1: acetone / 18 h / 20 °C

2: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 2 h / 20 °C

With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; acetone;