2-[[5-[[(2,3-dichlorophenyl)sulfonyl][[2-(trimethylsilyl)ethoxy]methyl]amino]-6-methoxypyrazin-2-yl]thio]-N-methoxy-N-methyl-acetamide

Base Information

Chemical Name:2-[[5-[[(2,3-dichlorophenyl)sulfonyl][[2-(trimethylsilyl)ethoxy]methyl]amino]-6-methoxypyrazin-2-yl]thio]-N-methoxy-N-methyl-acetamide
CAS No.:808139-27-7
Molecular Formula:C₂₁H₃₀Cl₂N₄O₆S₂Si
Molecular Weight:597.616
Hs Code.:

Synonyms:2-[[5-[[(2,3-dichlorophenyl)sulfonyl][[2-(trimethylsilyl)ethoxy]methyl]amino]-6-methoxypyrazin-2-yl]thio]-N-methoxy-N-methyl-acetamide

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Chemical Property of 2-[[5-[[(2,3-dichlorophenyl)sulfonyl][[2-(trimethylsilyl)ethoxy]methyl]amino]-6-methoxypyrazin-2-yl]thio]-N-methoxy-N-methyl-acetamide

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Technology Process of 2-[[5-[[(2,3-dichlorophenyl)sulfonyl][[2-(trimethylsilyl)ethoxy]methyl]amino]-6-methoxypyrazin-2-yl]thio]-N-methoxy-N-methyl-acetamide

There total 6 articles about 2-[[5-[[(2,3-dichlorophenyl)sulfonyl][[2-(trimethylsilyl)ethoxy]methyl]amino]-6-methoxypyrazin-2-yl]thio]-N-methoxy-N-methyl-acetamide 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:

: C₁₇H₂₃Cl₂N₃O₄S₂Si

: 67442-07-3
2-chloro-N-methoxy-N-methylacetamide

: 808139-27-7
2-[[5-[[(2,3-dichlorophenyl)sulfonyl][[2-(trimethylsilyl)ethoxy]methyl]amino]-6-methoxypyrazin-2-yl]thio]-N-methoxy-N-methyl-acetamide

Guidance literature:: With potassium tert-butylate; In tetrahydrofuran; at 20 ℃; for 1h;

Reference yield:

: 566203-62-1
2,3-dichloro-N-(5-chloro-3-methoxy-2-pyrazinyl)benzenesulphonamide

: 808139-27-7
2-[[5-[[(2,3-dichlorophenyl)sulfonyl][[2-(trimethylsilyl)ethoxy]methyl]amino]-6-methoxypyrazin-2-yl]thio]-N-methoxy-N-methyl-acetamide

Guidance literature:: Multi-step reaction with 4 steps

1: N-ethyl-N,N-diisopropylamine / dichloromethane / 0.5 h / 20 °C

2: caesium carbonate / acetonitrile / 24 h / 20 °C

3: potassium tert-butylate / tetrahydrofuran / 0.5 h

4: potassium tert-butylate / tetrahydrofuran / 1 h / 20 °C

With potassium tert-butylate; caesium carbonate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; acetonitrile;

Reference yield:

: 566204-86-2
2,3-dichloro-N-(5-chloro-3-methoxypyrazin-2-yl)-N-[[2-(trimethylsilyl)ethoxy]methyl]benzenesulfonamide

: 808139-27-7
2-[[5-[[(2,3-dichlorophenyl)sulfonyl][[2-(trimethylsilyl)ethoxy]methyl]amino]-6-methoxypyrazin-2-yl]thio]-N-methoxy-N-methyl-acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: caesium carbonate / acetonitrile / 24 h / 20 °C

2: potassium tert-butylate / tetrahydrofuran / 0.5 h

3: potassium tert-butylate / tetrahydrofuran / 1 h / 20 °C

With potassium tert-butylate; caesium carbonate; In tetrahydrofuran; acetonitrile;