4-{4-[(2-phenyl-5-ethyl-oxazole-4-carbonyl)-amino]-phenyl}-piperidine-1-carboxylic acid tert-butyl ester

Base Information

Chemical Name:4-{4-[(2-phenyl-5-ethyl-oxazole-4-carbonyl)-amino]-phenyl}-piperidine-1-carboxylic acid tert-butyl ester
CAS No.:1229419-52-6
Molecular Formula:C₂₈H₃₃N₃O₄
Molecular Weight:475.588
Hs Code.:

Synonyms:4-{4-[(2-phenyl-5-ethyl-oxazole-4-carbonyl)-amino]-phenyl}-piperidine-1-carboxylic acid tert-butyl ester

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Chemical Property of 4-{4-[(2-phenyl-5-ethyl-oxazole-4-carbonyl)-amino]-phenyl}-piperidine-1-carboxylic acid tert-butyl ester

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Technology Process of 4-{4-[(2-phenyl-5-ethyl-oxazole-4-carbonyl)-amino]-phenyl}-piperidine-1-carboxylic acid tert-butyl ester

There total 3 articles about 4-{4-[(2-phenyl-5-ethyl-oxazole-4-carbonyl)-amino]-phenyl}-piperidine-1-carboxylic acid tert-butyl 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:

Reference yield:

: 170011-57-1
tert-butyl 4-(4-aminophenyl)piperidin-1-carboxylate

: 138676-18-3
5-ethyl-2-phenyloxazole-4-carboxylic acid

: 1229419-52-6
4-{4-[(2-phenyl-5-ethyl-oxazole-4-carbonyl)-amino]-phenyl}-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; In dimethyl sulfoxide; at 20 ℃; for 1h;

Reference yield:

: 1229419-49-1
2-benzoylamino-4-methyl-3-oxo-butanoic acid benzyl ester

: 1229419-52-6
4-{4-[(2-phenyl-5-ethyl-oxazole-4-carbonyl)-amino]-phenyl}-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: iodine; triethylamine; triphenylphosphine / tetrahydrofuran / 1.17 h / -78 - 20 °C

2: hydrogen / palladium 10% on activated carbon / ethanol / 2 h / 20 °C / 1551.49 Torr

3: (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine / dimethyl sulfoxide / 1 h / 20 °C

With hydrogen; iodine; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; triphenylphosphine; palladium 10% on activated carbon; In tetrahydrofuran; ethanol; dimethyl sulfoxide;

Reference yield:

: 98-88-4
benzoyl chloride

: 1229419-52-6
4-{4-[(2-phenyl-5-ethyl-oxazole-4-carbonyl)-amino]-phenyl}-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: pyridine / dichloromethane / 1 h / 20 °C / Cooling with ice

2: iodine; triethylamine; triphenylphosphine / tetrahydrofuran / 1.17 h / -78 - 20 °C

3: hydrogen / palladium 10% on activated carbon / ethanol / 2 h / 20 °C / 1551.49 Torr

4: (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine / dimethyl sulfoxide / 1 h / 20 °C

With pyridine; hydrogen; iodine; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; triphenylphosphine; palladium 10% on activated carbon; In tetrahydrofuran; ethanol; dichloromethane; dimethyl sulfoxide;