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1-Piperidinecarboxylic acid, 4-[4-[1-[(dimethylamino)sulfonyl]-3-methyl-1H-pyrazol-4-yl]phenyl]-4-[(3- methoxyphenoxy)methyl]-, 1,1-dimethylethyl ester

Base Information Edit
  • Chemical Name:1-Piperidinecarboxylic acid, 4-[4-[1-[(dimethylamino)sulfonyl]-3-methyl-1H-pyrazol-4-yl]phenyl]-4-[(3- methoxyphenoxy)methyl]-, 1,1-dimethylethyl ester
  • CAS No.:917899-11-7
  • Molecular Formula:C30H40N4O6S
  • Molecular Weight:584.737
  • Hs Code.:
  • Mol file:917899-11-7.mol
1-Piperidinecarboxylic acid,
4-[4-[1-[(dimethylamino)sulfonyl]-3-methyl-1H-pyrazol-4-yl]phenyl]-4-[(3-
methoxyphenoxy)methyl]-, 1,1-dimethylethyl ester

Synonyms:

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Chemical Property of 1-Piperidinecarboxylic acid, 4-[4-[1-[(dimethylamino)sulfonyl]-3-methyl-1H-pyrazol-4-yl]phenyl]-4-[(3- methoxyphenoxy)methyl]-, 1,1-dimethylethyl ester Edit
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Technology Process of 1-Piperidinecarboxylic acid, 4-[4-[1-[(dimethylamino)sulfonyl]-3-methyl-1H-pyrazol-4-yl]phenyl]-4-[(3- methoxyphenoxy)methyl]-, 1,1-dimethylethyl ester

There total 9 articles about 1-Piperidinecarboxylic acid, 4-[4-[1-[(dimethylamino)sulfonyl]-3-methyl-1H-pyrazol-4-yl]phenyl]-4-[(3- methoxyphenoxy)methyl]-, 1,1-dimethylethyl ester 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:
Guidance literature:
3-methyl-1-sulphonic acid dimethylamide-pyrazole-4-boronic acid; 4-(4-bromo-phenyl)-4-(3-methoxy-phenoxymethyl)-piperidine-1-carboxylic acid tert-butyl ester; With potassium phosphate; tetrakis(triphenylphosphine) palladium(0); In methanol; ethanol; water; toluene; at 90 ℃;
In methanol; ethanol; water; toluene; at 20 - 90 ℃; for 3h;
Guidance literature:
Multi-step reaction with 3 steps
1.1: triethylamine / N,N-dimethyl-formamide / 3.5 h / 20 °C
2.1: caesium carbonate / N,N-dimethyl-formamide / 28 h / 50 - 100 °C
3.1: potassium phosphate / tetrakis(triphenylphosphine) palladium(0) / methanol; ethanol; water; toluene / 90 °C
3.2: bis(tri-tert-butyl)phosphine / 3 h / 20 - 90 °C
With potassium phosphate; caesium carbonate; triethylamine; tetrakis(triphenylphosphine) palladium(0); In methanol; ethanol; water; N,N-dimethyl-formamide; toluene;
Guidance literature:
Multi-step reaction with 5 steps
1.1: pyridine; carbon tetrabromide; triphenylphosphine / 1.5 h / 60 °C
2.1: morpholine; 1,8-diazabicyclo[5.4.0]undec-7-ene / dichloromethane / 2 h
3.1: triethylamine / N,N-dimethyl-formamide / 3.5 h / 20 °C
4.1: caesium carbonate / N,N-dimethyl-formamide / 28 h / 50 - 100 °C
5.1: potassium phosphate / tetrakis(triphenylphosphine) palladium(0) / methanol; ethanol; water; toluene / 90 °C
5.2: bis(tri-tert-butyl)phosphine / 3 h / 20 - 90 °C
With morpholine; pyridine; potassium phosphate; carbon tetrabromide; caesium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; triphenylphosphine; tetrakis(triphenylphosphine) palladium(0); In methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide; toluene;
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