4-[4-(4-methanesulfonylphenoxymethyl)thiazol-2-yl]-4-methylpiperidine-1-carboxylic acid tert-butyl ester

Base Information

Chemical Name:4-[4-(4-methanesulfonylphenoxymethyl)thiazol-2-yl]-4-methylpiperidine-1-carboxylic acid tert-butyl ester
CAS No.:1037792-97-4
Molecular Formula:C₂₂H₃₀N₂O₅S₂
Molecular Weight:466.623
Hs Code.:

Synonyms:4-[4-(4-methanesulfonylphenoxymethyl)thiazol-2-yl]-4-methylpiperidine-1-carboxylic acid tert-butyl ester

Suppliers and Price of 4-[4-(4-methanesulfonylphenoxymethyl)thiazol-2-yl]-4-methylpiperidine-1-carboxylic acid tert-butyl 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 4-[4-(4-methanesulfonylphenoxymethyl)thiazol-2-yl]-4-methylpiperidine-1-carboxylic acid tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 4-[4-(4-methanesulfonylphenoxymethyl)thiazol-2-yl]-4-methylpiperidine-1-carboxylic acid tert-butyl ester

There total 7 articles about 4-[4-(4-methanesulfonylphenoxymethyl)thiazol-2-yl]-4-methylpiperidine-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:

: 1044136-47-1
4-(4-methanesulfonyloxymethylthiazol-2-yl)-4-methylpiperidine-1-carboxylic acid tert-butyl ester

: 14763-60-1
4-methanesulfonyl-phenol

: 1037792-97-4
4-[4-(4-methanesulfonylphenoxymethyl)thiazol-2-yl]-4-methylpiperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: With caesium carbonate; In acetonitrile; at 40 ℃;

Reference yield:

: 530115-96-9
4-cyano-4-methylpiperidine-1-carboxylic acid tert-butyl ester

: 1037792-97-4
4-[4-(4-methanesulfonylphenoxymethyl)thiazol-2-yl]-4-methylpiperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium hydroxide; dihydrogen peroxide / methanol; dimethyl sulfoxide; water / 3 h / 50 °C

2.1: Lawessons reagent / tetrahydrofuran / 3 h / 50 °C

3.1: ethanol / 3 h / Reflux

3.2: 20 °C

4.1: lithium aluminium tetrahydride / tetrahydrofuran / 2 h / 0 °C

5.1: triethylamine / dichloromethane / 1 h / 0 °C

6.1: caesium carbonate / acetonitrile / 40 °C

With Lawessons reagent; lithium aluminium tetrahydride; dihydrogen peroxide; caesium carbonate; triethylamine; sodium hydroxide; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; dimethyl sulfoxide; acetonitrile;

Reference yield:

: 91419-52-2
1-tert-butoxycarbonyl-4-cyanopiperidine

: 1037792-97-4
4-[4-(4-methanesulfonylphenoxymethyl)thiazol-2-yl]-4-methylpiperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 7 steps

1.1: lithium hexamethyldisilazane / tetrahydrofuran / 1 h / 0 °C

1.2: 2 h / 0 °C

2.1: sodium hydroxide; dihydrogen peroxide / methanol; dimethyl sulfoxide; water / 3 h / 50 °C

3.1: Lawessons reagent / tetrahydrofuran / 3 h / 50 °C

4.1: ethanol / 3 h / Reflux

4.2: 20 °C

5.1: lithium aluminium tetrahydride / tetrahydrofuran / 2 h / 0 °C

6.1: triethylamine / dichloromethane / 1 h / 0 °C

7.1: caesium carbonate / acetonitrile / 40 °C

With Lawessons reagent; lithium aluminium tetrahydride; dihydrogen peroxide; caesium carbonate; triethylamine; sodium hydroxide; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; dimethyl sulfoxide; acetonitrile;