(S)-tert-butyl-4-(1-amino-3-(4-iodophenyl)-1-oxopropan-2-yl carbamoyl)tetrahydro-2H-pyran-4-yl carbamate

Base Information

Chemical Name:(S)-tert-butyl-4-(1-amino-3-(4-iodophenyl)-1-oxopropan-2-yl carbamoyl)tetrahydro-2H-pyran-4-yl carbamate
CAS No.:1254318-91-6
Molecular Formula:C₂₀H₂₈IN₃O₅
Molecular Weight:517.364
Hs Code.:

Synonyms:(S)-tert-butyl-4-(1-amino-3-(4-iodophenyl)-1-oxopropan-2-yl carbamoyl)tetrahydro-2H-pyran-4-yl carbamate

Suppliers and Price of (S)-tert-butyl-4-(1-amino-3-(4-iodophenyl)-1-oxopropan-2-yl carbamoyl)tetrahydro-2H-pyran-4-yl carbamate

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 (S)-tert-butyl-4-(1-amino-3-(4-iodophenyl)-1-oxopropan-2-yl carbamoyl)tetrahydro-2H-pyran-4-yl carbamate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (S)-tert-butyl-4-(1-amino-3-(4-iodophenyl)-1-oxopropan-2-yl carbamoyl)tetrahydro-2H-pyran-4-yl carbamate

There total 1 articles about (S)-tert-butyl-4-(1-amino-3-(4-iodophenyl)-1-oxopropan-2-yl carbamoyl)tetrahydro-2H-pyran-4-yl carbamate 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: 96.0%

: 172843-97-9
4-(Boc-amino)tetrahydropyran-4-carboxylic acid

: 97964-72-2
(S)-2-amino-3-(4-iodophenyl)propionamamide

: 1254318-91-6
(S)-tert-butyl-4-(1-amino-3-(4-iodophenyl)-1-oxopropan-2-yl carbamoyl)tetrahydro-2H-pyran-4-yl carbamate

Guidance literature:: With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1021/jm401705g

Reference yield: 77.0%

: 1254318-91-6
(S)-tert-butyl-4-(1-amino-3-(4-iodophenyl)-1-oxopropan-2-yl carbamoyl)tetrahydro-2H-pyran-4-yl carbamate

: (4-cyano[¹³C₆]phenyl)boronic acid

: tert-butyl N-[4-[[(1S)-2-amino-1-[[4-(4-cyano[¹³C₆]phenyl)phenyl]methyl]-2-oxoethyl]carbamoyl]tetrahydropyran-4-yl]carbamate

Guidance literature:: With dichloro[1,1′-bis[bis(1,1-dimethylethyl)phosphino]ferrocene-P,P′]palladium; potassium carbonate; In water; acetonitrile; at 80 ℃; for 5h; Inert atmosphere;
DOI:10.1002/jlcr.3483

Reference yield: 69.2%

: 1254318-91-6
(S)-tert-butyl-4-(1-amino-3-(4-iodophenyl)-1-oxopropan-2-yl carbamoyl)tetrahydro-2H-pyran-4-yl carbamate

: 73183-34-3
bis(pinacol)diborane

: 1254319-24-8
(S)-tert-butyl-4-(1-amino-1-oxo-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propan-2-yl carbamoyl)tetrahydro-2H-pyran-4-yl carbamate

Guidance literature:: With dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II); potassium acetate; In water; acetonitrile; for 48h; Inert atmosphere; Reflux;
DOI:10.1021/jm401705g