tert-butyl N-(N-{4-[(1-tert-butoxycarbonyl-4-piperidyl)oxy]phenyl}-N-[(7-cyano-2-naphthyl)methyl]sulfamoyl)-N-methylcarbamate

Base Information

Chemical Name:tert-butyl N-(N-{4-[(1-tert-butoxycarbonyl-4-piperidyl)oxy]phenyl}-N-[(7-cyano-2-naphthyl)methyl]sulfamoyl)-N-methylcarbamate
CAS No.:454437-46-8
Molecular Formula:C₃₄H₄₂N₄O₇S
Molecular Weight:650.796
Hs Code.:

Synonyms:tert-butyl N-(N-{4-[(1-tert-butoxycarbonyl-4-piperidyl)oxy]phenyl}-N-[(7-cyano-2-naphthyl)methyl]sulfamoyl)-N-methylcarbamate

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Chemical Property of tert-butyl N-(N-{4-[(1-tert-butoxycarbonyl-4-piperidyl)oxy]phenyl}-N-[(7-cyano-2-naphthyl)methyl]sulfamoyl)-N-methylcarbamate

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Technology Process of tert-butyl N-(N-{4-[(1-tert-butoxycarbonyl-4-piperidyl)oxy]phenyl}-N-[(7-cyano-2-naphthyl)methyl]sulfamoyl)-N-methylcarbamate

There total 8 articles about tert-butyl N-(N-{4-[(1-tert-butoxycarbonyl-4-piperidyl)oxy]phenyl}-N-[(7-cyano-2-naphthyl)methyl]sulfamoyl)-N-methylcarbamate 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: 87.0%

: 67-56-1
methanol

: 179756-31-1
tert-butyl N-(N-{4-[(1-tert-butoxycarbonyl-4-piperidyl)oxy]phenyl}-N-[(7-cyano-2-naphthyl)methyl]sulfamoyl)carbamate

: 454437-46-8
tert-butyl N-(N-{4-[(1-tert-butoxycarbonyl-4-piperidyl)oxy]phenyl}-N-[(7-cyano-2-naphthyl)methyl]sulfamoyl)-N-methylcarbamate

Guidance literature:: With triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; at 20 ℃; for 0.666667h;
DOI:10.1016/S0968-0896(01)00418-7

Reference yield:

: 1972-28-7,218603-74-8
diethylazodicarboxylate

: 179756-31-1
tert-butyl N-(N-{4-[(1-tert-butoxycarbonyl-4-piperidyl)oxy]phenyl}-N-[(7-cyano-2-naphthyl)methyl]sulfamoyl)carbamate

: 454437-46-8
tert-butyl N-(N-{4-[(1-tert-butoxycarbonyl-4-piperidyl)oxy]phenyl}-N-[(7-cyano-2-naphthyl)methyl]sulfamoyl)-N-methylcarbamate

Guidance literature:: With triphenylphosphine; In tetrahydrofuran; methanol; hexane; ethyl acetate;

Reference yield:

: 100-02-7,78813-13-5,89830-32-0
4-nitro-phenol

: 454437-46-8
tert-butyl N-(N-{4-[(1-tert-butoxycarbonyl-4-piperidyl)oxy]phenyl}-N-[(7-cyano-2-naphthyl)methyl]sulfamoyl)-N-methylcarbamate

Guidance literature:: Multi-step reaction with 5 steps

1: 77 percent / Ph₃P; DEAD / tetrahydrofuran / 21 h / 20 °C

2: 98 percent / H₂ / 10 percent Pd/C / ethanol / 15 h / 20 °C

3: 79 percent / NaB(OAc)3H / CH₂Cl₂; acetic acid / 0.75 h / 20 °C

4: 89 percent / pyridine / 15 h / 3 °C

5: 87 percent / Ph₃P; DEAD / tetrahydrofuran / 0.67 h / 20 °C

With pyridine; hydrogen; sodium tris(acetoxy)borohydride; triphenylphosphine; diethylazodicarboxylate; palladium on activated charcoal; In tetrahydrofuran; ethanol; dichloromethane; acetic acid; 1: Mitsunobu condensation;
DOI:10.1016/S0968-0896(01)00418-7