N-[(3-Hydroxy-2-pyridinyl)carbonyl]cyclo[L-Thr*-D-Ala-L-Pro-N-methyl-L-Phe-4-oxo-L-pipecoloyl-L-phenyl Gly-]

Base Information

Chemical Name:N-[(3-Hydroxy-2-pyridinyl)carbonyl]cyclo[L-Thr*-D-Ala-L-Pro-N-methyl-L-Phe-4-oxo-L-pipecoloyl-L-phenyl Gly-]
CAS No.:33477-37-1
Molecular Formula:C₄₂H₄₇N₇O₁₀
Molecular Weight:809.876
Hs Code.:
Mol file:33477-37-1.mol

Synonyms:VirginiamycinS1, 2-D-alanine-;12H-Pyrido[2,1-f]pyrrolo[2,1-l][1,4,7,10,13,16]oxapentaazacyclononadecine,cyclic peptide deriv.; Glycine,N-[(3-hydroxy-2-pyridinyl)carbonyl]-L-threonyl-D-alanyl-L-prolyl-N-methyl-L-phenylalanyl-4-oxo-L-2-piperidinecarbonyl-L-2-phenyl-,r-lactone; Staphylomycin S4

Suppliers and Price of N-[(3-Hydroxy-2-pyridinyl)carbonyl]cyclo[L-Thr*-D-Ala-L-Pro-N-methyl-L-Phe-4-oxo-L-pipecoloyl-L-phenyl Gly-]

Supply Marketing:

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

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Chemical Property of N-[(3-Hydroxy-2-pyridinyl)carbonyl]cyclo[L-Thr*-D-Ala-L-Pro-N-methyl-L-Phe-4-oxo-L-pipecoloyl-L-phenyl Gly-]

Chemical Property:

PSA：224.72000
LogP:1.67610

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of N-[(3-Hydroxy-2-pyridinyl)carbonyl]cyclo[L-Thr*-D-Ala-L-Pro-N-methyl-L-Phe-4-oxo-L-pipecoloyl-L-phenyl Gly-]

There total 2 articles about N-[(3-Hydroxy-2-pyridinyl)carbonyl]cyclo[L-Thr*-D-Ala-L-Pro-N-methyl-L-Phe-4-oxo-L-pipecoloyl-L-phenyl Gly-] 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:

: 102410-85-5
Pic(3-OH)-Thr(Boc-MePhe-4Kps-Phg-)-D-Ala-Pro-OBu^t

: 33477-37-1
Virginiamycin S₄

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / 6.1 N HCl / CH₂Cl₂; dioxane / 3 h / Ambient temperature

2: 1) NMM, 2) EDCI, DMAP / 1) CH₂Cl₂, 3 min, 2) CH₂Cl₂, 3 d, -2 deg C, 3 d, room temp.

With 4-methyl-morpholine; hydrogenchloride; dmap; In 1,4-dioxane; dichloromethane;
DOI:10.1002/jlac.198619860102

Reference yield:

: 102410-86-6
Pic(3-OH)-Thr(H-MePhe-4Kps-Phg-)-D-Ala-Pro-OH*2HCl

: 33477-37-1
Virginiamycin S₄

Guidance literature:: With 4-methyl-morpholine; dmap; Yield given. Multistep reaction; 1) CH₂Cl₂, 3 min, 2) CH₂Cl₂, 3 d, -2 deg C, 3 d, room temp.;
DOI:10.1002/jlac.198619860102