2-({1-[2-(2-[(3-Allyloxycarbonyloxy-pyridine-2-carbonyl)-amino]-3-{2-[(4-oxo-piperidine-2-carbonyl)-amino]-2-phenyl-acetoxy}-butyrylamino)-butyryl]-pyrrolidine-2-carbonyl}-methyl-amino)-3-phenyl-propionic acid; compound with trifluoro-acetic acid

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Chemical Name:2-({1-[2-(2-[(3-Allyloxycarbonyloxy-pyridine-2-carbonyl)-amino]-3-{2-[(4-oxo-piperidine-2-carbonyl)-amino]-2-phenyl-acetoxy}-butyrylamino)-butyryl]-pyrrolidine-2-carbonyl}-methyl-amino)-3-phenyl-propionic acid; compound with trifluoro-acetic acid
CAS No.:127092-13-1
Molecular Formula:C₂HF₃O₂*C₄₇H₅₅N₇O₁₃
Molecular Weight:1040.02
Hs Code.:

2-({1-[2-(2-[(3-Allyloxycarbonyloxy-pyridine-2-carbonyl)-amino]-3-{2-[(4-oxo-piperidine-2-carbonyl)-amino]-2-phenyl-acetoxy}-butyrylamino)-butyryl]-pyrrolidine-2-carbonyl}-methyl-amino)-3-phenyl-propionic acid; compound with trifluoro-acetic acid

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Chemical Property of 2-({1-[2-(2-[(3-Allyloxycarbonyloxy-pyridine-2-carbonyl)-amino]-3-{2-[(4-oxo-piperidine-2-carbonyl)-amino]-2-phenyl-acetoxy}-butyrylamino)-butyryl]-pyrrolidine-2-carbonyl}-methyl-amino)-3-phenyl-propionic acid; compound with trifluoro-acetic acid

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Technology Process of 2-({1-[2-(2-[(3-Allyloxycarbonyloxy-pyridine-2-carbonyl)-amino]-3-{2-[(4-oxo-piperidine-2-carbonyl)-amino]-2-phenyl-acetoxy}-butyrylamino)-butyryl]-pyrrolidine-2-carbonyl}-methyl-amino)-3-phenyl-propionic acid; compound with trifluoro-acetic acid

There total 3 articles about 2-({1-[2-(2-[(3-Allyloxycarbonyloxy-pyridine-2-carbonyl)-amino]-3-{2-[(4-oxo-piperidine-2-carbonyl)-amino]-2-phenyl-acetoxy}-butyrylamino)-butyryl]-pyrrolidine-2-carbonyl}-methyl-amino)-3-phenyl-propionic acid; compound with trifluoro-acetic acid 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:

: 668-72-4,23152-29-6,117603-96-0
virginiamycin S₁

: 127092-13-1
2-({1-[2-(2-[(3-Allyloxycarbonyloxy-pyridine-2-carbonyl)-amino]-3-{2-[(4-oxo-piperidine-2-carbonyl)-amino]-2-phenyl-acetoxy}-butyrylamino)-butyryl]-pyrrolidine-2-carbonyl}-methyl-amino)-3-phenyl-propionic acid; compound with trifluoro-acetic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 1,8-bis(dimethylamino)naphthalene / CH₂Cl₂ / 10 h

2: 81 percent / 80 h / Ambient temperature

With N,N,N',N'-tetramethyl-1,8-diaminonaphthalene; In dichloromethane;

Reference yield:

: 127106-17-6
Carbonic acid 2-(3-benzyl-12-ethyl-4,16-dimethyl-2,5,11,14,18,21,24-heptaoxo-19-phenyl-17-oxa-1,4,10,13,20-pentaaza-tricyclo[20.4.0.0^6,10]hexacos-15-ylcarbamoyl)-pyridin-3-yl ester 2,2,2-trichloro-ethyl ester

: 127092-13-1
2-({1-[2-(2-[(3-Allyloxycarbonyloxy-pyridine-2-carbonyl)-amino]-3-{2-[(4-oxo-piperidine-2-carbonyl)-amino]-2-phenyl-acetoxy}-butyrylamino)-butyryl]-pyrrolidine-2-carbonyl}-methyl-amino)-3-phenyl-propionic acid; compound with trifluoro-acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 90 percent / Zn / methanol / 1 h / Heating

2: 1,8-bis(dimethylamino)naphthalene / CH₂Cl₂ / 10 h

3: 81 percent / 80 h / Ambient temperature

With N,N,N',N'-tetramethyl-1,8-diaminonaphthalene; zinc; In methanol; dichloromethane;

Reference yield:

: 127092-11-9
3-(2,4-Dinitro-phenoxy)-pyridine-2-carboxylic acid (3-benzyl-12-ethyl-4,16-dimethyl-2,5,11,14,18,21,24-heptaoxo-19-phenyl-17-oxa-1,4,10,13,20-pentaaza-tricyclo[20.4.0.0^6,10]hexacos-15-yl)-amide

: 127092-13-1
2-({1-[2-(2-[(3-Allyloxycarbonyloxy-pyridine-2-carbonyl)-amino]-3-{2-[(4-oxo-piperidine-2-carbonyl)-amino]-2-phenyl-acetoxy}-butyrylamino)-butyryl]-pyrrolidine-2-carbonyl}-methyl-amino)-3-phenyl-propionic acid; compound with trifluoro-acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 82 percent / thiophenol, triethylamine / CH₂Cl₂ / 0.12 h

2: 1,8-bis(dimethylamino)naphthalene / CH₂Cl₂ / 10 h

3: 81 percent / 80 h / Ambient temperature

With N,N,N',N'-tetramethyl-1,8-diaminonaphthalene; thiophenol; triethylamine; In dichloromethane;