ethyl 1-[1-(tert-butoxycarbonyl)-(4S)-fluoro-(2S)-pyrrolidinylcarbonyl]-4-piperidinylacetate

Base Information

Chemical Name:ethyl 1-[1-(tert-butoxycarbonyl)-(4S)-fluoro-(2S)-pyrrolidinylcarbonyl]-4-piperidinylacetate
CAS No.:441714-17-6
Molecular Formula:C₁₉H₃₁FN₂O₅
Molecular Weight:386.464
Hs Code.:

Synonyms:ethyl 1-[1-(tert-butoxycarbonyl)-(4S)-fluoro-(2S)-pyrrolidinylcarbonyl]-4-piperidinylacetate

Suppliers and Price of ethyl 1-[1-(tert-butoxycarbonyl)-(4S)-fluoro-(2S)-pyrrolidinylcarbonyl]-4-piperidinylacetate

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 ethyl 1-[1-(tert-butoxycarbonyl)-(4S)-fluoro-(2S)-pyrrolidinylcarbonyl]-4-piperidinylacetate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of ethyl 1-[1-(tert-butoxycarbonyl)-(4S)-fluoro-(2S)-pyrrolidinylcarbonyl]-4-piperidinylacetate

There total 1 articles about ethyl 1-[1-(tert-butoxycarbonyl)-(4S)-fluoro-(2S)-pyrrolidinylcarbonyl]-4-piperidinylacetate 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: 32.0%

: 59184-90-6
ethyl (piperidin-4-yl)acetate

: 203866-13-1
(2S,4S)-1-(tert-butoxycarbonyl)-4-fluoropyrrolidine-2-carboxylic acid

: 441714-17-6
ethyl 1-[1-(tert-butoxycarbonyl)-(4S)-fluoro-(2S)-pyrrolidinylcarbonyl]-4-piperidinylacetate

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In tetrahydrofuran; at 20 ℃; for 16h;
DOI:10.1016/j.bmc.2008.12.026