diprop-2-enyl N-<(4-<amino>phenyl)carbamoyloxy>methyl>phenoxy)carbamoyl>-L-glutamate

Base Information

Chemical Name:diprop-2-enyl N-<(4-<amino>phenyl)carbamoyloxy>methyl>phenoxy)carbamoyl>-L-glutamate
CAS No.:219591-93-2
Molecular Formula:C₃₀H₃₆F₂N₄O₇
Molecular Weight:602.635
Hs Code.:

diprop-2-enyl N-<(4-<<N-(4-<bis<2-fluoroethyl>amino>phenyl)carbamoyloxy>methyl>phenoxy)carbamoyl>-L-glutamate

Synonyms:diprop-2-enyl N-<(4-<amino>phenyl)carbamoyloxy>methyl>phenoxy)carbamoyl>-L-glutamate

Suppliers and Price of diprop-2-enyl N-<(4-<amino>phenyl)carbamoyloxy>methyl>phenoxy)carbamoyl>-L-glutamate

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 diprop-2-enyl N-<(4-<amino>phenyl)carbamoyloxy>methyl>phenoxy)carbamoyl>-L-glutamate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of diprop-2-enyl N-<(4-<amino>phenyl)carbamoyloxy>methyl>phenoxy)carbamoyl>-L-glutamate

There total 11 articles about diprop-2-enyl N-<(4-<amino>phenyl)carbamoyloxy>methyl>phenoxy)carbamoyl>-L-glutamate 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:

: 18226-17-0
N,N-bis(2-hydroxyethyl)-4-nitroaniline

: 219591-93-2
diprop-2-enyl N-<(4-<amino>phenyl)carbamoyloxy>methyl>phenoxy)carbamoyl>-L-glutamate

Guidance literature:: Multi-step reaction with 5 steps

1: Et₃N, 4-(dimethylamino)pyridine / CH₂Cl₂ / 1 h

2: Amberlyst 26 F^- / CHCl₃ / 72 h / Heating

3: 84 percent / ammonium formate / 10 percent Pd/C / ethanol / 1.5 h / Ambient temperature

4: Et₃N / CH₂Cl₂ / 0.25 h

5: dibutyltin dilaurate / toluene / 12 h / Ambient temperature

With dmap; dibutyltin(II) dilaurate; Amberlyst 26 F^-; ammonium formate; triethylamine; palladium on activated charcoal; In ethanol; dichloromethane; chloroform; toluene;
DOI:10.1021/jm980425k

Reference yield:

: 219591-97-6
4-nitrobenzene

: 219591-93-2
diprop-2-enyl N-<(4-<amino>phenyl)carbamoyloxy>methyl>phenoxy)carbamoyl>-L-glutamate

Guidance literature:: Multi-step reaction with 3 steps

1: 84 percent / ammonium formate / 10 percent Pd/C / ethanol / 1.5 h / Ambient temperature

2: Et₃N / CH₂Cl₂ / 0.25 h

3: dibutyltin dilaurate / toluene / 12 h / Ambient temperature

With dibutyltin(II) dilaurate; ammonium formate; triethylamine; palladium on activated charcoal; In ethanol; dichloromethane; toluene;
DOI:10.1021/jm980425k

Reference yield:

: 18483-99-3
2-(4-nitrobenzyloxy)tetrahydro-2H-pyran

: 219591-93-2
diprop-2-enyl N-<(4-<amino>phenyl)carbamoyloxy>methyl>phenoxy)carbamoyl>-L-glutamate

Guidance literature:: Multi-step reaction with 4 steps

1: 38 percent / ammonium formate / 10 percent Pd/C / ethanol / 1.5 h / 20 °C

2: Et₃N / toluene

3: 45 percent / aq. AcOH / tetrahydrofuran / 3.5 h / 45 °C

4: dibutyltin dilaurate / toluene / 12 h / Ambient temperature

With dibutyltin(II) dilaurate; ammonium formate; acetic acid; triethylamine; palladium on activated charcoal; In tetrahydrofuran; ethanol; toluene;
DOI:10.1021/jm980425k