2-(Methoxycarbonylmethyl-carbamoyl)-2-(2-oxo-ethyl)-piperidine-1-carboxylic acid benzyl ester

Base Information

Chemical Name:2-(Methoxycarbonylmethyl-carbamoyl)-2-(2-oxo-ethyl)-piperidine-1-carboxylic acid benzyl ester
CAS No.:1026155-18-9
Molecular Formula:C₁₉H₂₄N₂O₆
Molecular Weight:376.409
Hs Code.:

Synonyms:2-(Methoxycarbonylmethyl-carbamoyl)-2-(2-oxo-ethyl)-piperidine-1-carboxylic acid benzyl ester

Suppliers and Price of 2-(Methoxycarbonylmethyl-carbamoyl)-2-(2-oxo-ethyl)-piperidine-1-carboxylic acid benzyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 2-(Methoxycarbonylmethyl-carbamoyl)-2-(2-oxo-ethyl)-piperidine-1-carboxylic acid benzyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-(Methoxycarbonylmethyl-carbamoyl)-2-(2-oxo-ethyl)-piperidine-1-carboxylic acid benzyl ester

There total 7 articles about 2-(Methoxycarbonylmethyl-carbamoyl)-2-(2-oxo-ethyl)-piperidine-1-carboxylic acid benzyl 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:

: 71170-89-3
N-(benzyloxycarbonyl)-DL-pipecolinic acid tert-butyl ester

: 1026155-18-9
2-(Methoxycarbonylmethyl-carbamoyl)-2-(2-oxo-ethyl)-piperidine-1-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) LDA / 1.) THF, hexane, EtPh, -78 deg C, 20 min, 2.) -78 deg C, 20 min

2: CF₃CO₂H / CH₂Cl₂ / 3 h / Ambient temperature

3: HOBt, NEt₃, dicyclohexylcarbodiimide (DCC) / CHCl₃ / Ambient temperature

4: 1.) OsO₄, H₂O, 2.) NaIO₄ / 1.) MeOH, 10 min, room temperature, 2.) 2 h

With sodium periodate; osmium(VIII) oxide; water; benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide; trifluoroacetic acid; lithium diisopropyl amide; In dichloromethane; chloroform;
DOI:10.1021/jo00056a018

Reference yield:

: 28697-07-6
N-benzyloxycarbonyl D/L-pipecolinic acid

: 1026155-18-9
2-(Methoxycarbonylmethyl-carbamoyl)-2-(2-oxo-ethyl)-piperidine-1-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 58 percent / H₂SO₄ / diethyl ether / 24 h / Ambient temperature

2: 1.) LDA / 1.) THF, hexane, EtPh, -78 deg C, 20 min, 2.) -78 deg C, 20 min

3: CF₃CO₂H / CH₂Cl₂ / 3 h / Ambient temperature

4: HOBt, NEt₃, dicyclohexylcarbodiimide (DCC) / CHCl₃ / Ambient temperature

5: 1.) OsO₄, H₂O, 2.) NaIO₄ / 1.) MeOH, 10 min, room temperature, 2.) 2 h

With sodium periodate; osmium(VIII) oxide; sulfuric acid; water; benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide; trifluoroacetic acid; lithium diisopropyl amide; In diethyl ether; dichloromethane; chloroform;
DOI:10.1021/jo00056a018

Reference yield:

: 501-53-1,94274-21-2
benzyl chloroformate

: 1026155-18-9
2-(Methoxycarbonylmethyl-carbamoyl)-2-(2-oxo-ethyl)-piperidine-1-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 89 percent / 2 N NaOH / 1 h / < 5 deg C to room temperature

2: 58 percent / H₂SO₄ / diethyl ether / 24 h / Ambient temperature

3: 1.) LDA / 1.) THF, hexane, EtPh, -78 deg C, 20 min, 2.) -78 deg C, 20 min

4: CF₃CO₂H / CH₂Cl₂ / 3 h / Ambient temperature

5: HOBt, NEt₃, dicyclohexylcarbodiimide (DCC) / CHCl₃ / Ambient temperature

6: 1.) OsO₄, H₂O, 2.) NaIO₄ / 1.) MeOH, 10 min, room temperature, 2.) 2 h

With sodium hydroxide; sodium periodate; osmium(VIII) oxide; sulfuric acid; water; benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide; trifluoroacetic acid; lithium diisopropyl amide; In diethyl ether; dichloromethane; chloroform;
DOI:10.1021/jo00056a018