methyl 5-[(1-tert-butoxycarbonyl-4-piperidyl)oxy]-N-(tert-butoxycarbonylsulfamoyl)-N-{[(3-cyanophenyl)(methyl)carbamoyl]methyl}anthranilate

Base Information

Chemical Name:methyl 5-[(1-tert-butoxycarbonyl-4-piperidyl)oxy]-N-(tert-butoxycarbonylsulfamoyl)-N-{[(3-cyanophenyl)(methyl)carbamoyl]methyl}anthranilate
CAS No.:540765-43-3
Molecular Formula:C₃₃H₄₃N₅O₁₀S
Molecular Weight:701.798
Hs Code.:

methyl 5-[(1-tert-butoxycarbonyl-4-piperidyl)oxy]-N-(tert-butoxycarbonylsulfamoyl)-N-{[(3-cyanophenyl)(methyl)carbamoyl]methyl}anthranilate

Synonyms:methyl 5-[(1-tert-butoxycarbonyl-4-piperidyl)oxy]-N-(tert-butoxycarbonylsulfamoyl)-N-{[(3-cyanophenyl)(methyl)carbamoyl]methyl}anthranilate

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Chemical Property of methyl 5-[(1-tert-butoxycarbonyl-4-piperidyl)oxy]-N-(tert-butoxycarbonylsulfamoyl)-N-{[(3-cyanophenyl)(methyl)carbamoyl]methyl}anthranilate

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Technology Process of methyl 5-[(1-tert-butoxycarbonyl-4-piperidyl)oxy]-N-(tert-butoxycarbonylsulfamoyl)-N-{[(3-cyanophenyl)(methyl)carbamoyl]methyl}anthranilate

There total 6 articles about methyl 5-[(1-tert-butoxycarbonyl-4-piperidyl)oxy]-N-(tert-butoxycarbonylsulfamoyl)-N-{[(3-cyanophenyl)(methyl)carbamoyl]methyl}anthranilate 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: 95.0%

: 147000-89-3
N-tert-butyloxycarbonylsulfamoyl chloride

: 540765-42-2
methyl 5-[(1-tert-butoxycarbonyl-4-piperidyl)oxy]-N-{[(3-cyanophenyl)(methyl)carbamoyl]methyl}anthranilate

: 540765-43-3
methyl 5-[(1-tert-butoxycarbonyl-4-piperidyl)oxy]-N-(tert-butoxycarbonylsulfamoyl)-N-{[(3-cyanophenyl)(methyl)carbamoyl]methyl}anthranilate

Guidance literature:: In pyridine; at 20 ℃; for 1h;
DOI:10.1016/S0968-0896(02)00462-5

Reference yield:

: 64910-52-7
3-(methylamino)benzonitrile

: 540765-43-3
methyl 5-[(1-tert-butoxycarbonyl-4-piperidyl)oxy]-N-(tert-butoxycarbonylsulfamoyl)-N-{[(3-cyanophenyl)(methyl)carbamoyl]methyl}anthranilate

Guidance literature:: Multi-step reaction with 3 steps

1: 92 percent / NaHCO₃ / ethyl acetate; H₂O / 0.25 h / 20 °C

2: 35 percent / K₂CO₃ / acetonitrile / 12 h / Heating

3: 95 percent / pyridine / 1 h / 20 °C

With sodium hydrogencarbonate; potassium carbonate; In pyridine; water; ethyl acetate; acetonitrile;
DOI:10.1016/S0968-0896(02)00462-5

Reference yield:

: 1882-72-0
methyl 2-amino-5-hydroxybenzoate

: 540765-43-3
methyl 5-[(1-tert-butoxycarbonyl-4-piperidyl)oxy]-N-(tert-butoxycarbonylsulfamoyl)-N-{[(3-cyanophenyl)(methyl)carbamoyl]methyl}anthranilate

Guidance literature:: Multi-step reaction with 3 steps

1: 41 percent / PPh₃; DEAD / tetrahydrofuran / 96 h / 20 °C

2: 35 percent / K₂CO₃ / acetonitrile / 12 h / Heating

3: 95 percent / pyridine / 1 h / 20 °C

With potassium carbonate; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; pyridine; acetonitrile; 1: Mitsunobu condensation;
DOI:10.1016/S0968-0896(02)00462-5