Technology Process of Carbamic acid,
[2-[[(3R)-1-[[2'-[[[(1,1-dimethylethoxy)carbonyl]amino]methyl][1,1'-biphen
yl]-4-yl]methyl]-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepin-3-yl]amino]-1,
1-dimethyl-2-oxoethyl]-, phenylmethyl ester
There total 8 articles about Carbamic acid,
[2-[[(3R)-1-[[2'-[[[(1,1-dimethylethoxy)carbonyl]amino]methyl][1,1'-biphen
yl]-4-yl]methyl]-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepin-3-yl]amino]-1,
1-dimethyl-2-oxoethyl]-, phenylmethyl ester 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:
- Guidance literature:
-
Multi-step reaction with 5 steps
1: 1.) Et3N / 1.) methylene chloride, 0 deg C, 5 min, 2.) methylene chloride, 2 h
2: 100 percent / 5N aq. NaOH, Pd(PPh3)4 / benzene; propan-2-ol / 2 h / Heating
3: 92 percent / Bu4NF / tetrahydrofuran / 2 h / Ambient temperature
4: 97 percent / Et3N / CH2Cl2 / 2 h / 0 °C
5: 1.) NaH / 1.) DMF, 15 min, 2.) DMF, 0 deg C, 15 min
With
sodium hydroxide; tetrakis(triphenylphosphine) palladium(0); tetrabutyl ammonium fluoride; sodium hydride; triethylamine;
In
tetrahydrofuran; dichloromethane; isopropyl alcohol; benzene;
DOI:10.1021/jm970816j
- Guidance literature:
-
Multi-step reaction with 2 steps
1: Py, benzotriazol-1-yloxytripyrrolidinophosphonium hexafluorophosphate / CH2Cl2 / 2 h / Ambient temperature
2: 1.) NaH / 1.) DMF, 15 min, 2.) DMF, 0 deg C, 15 min
With
pyridine; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; sodium hydride;
In
dichloromethane;
DOI:10.1021/jm970816j
- Guidance literature:
-
Multi-step reaction with 5 steps
1: 1.) Et3N / 1.) methylene chloride, 0 deg C, 5 min, 2.) methylene chloride, 2 h
2: 100 percent / 5N aq. NaOH, Pd(PPh3)4 / benzene; propan-2-ol / 2 h / Heating
3: 92 percent / Bu4NF / tetrahydrofuran / 2 h / Ambient temperature
4: 97 percent / Et3N / CH2Cl2 / 2 h / 0 °C
5: 1.) NaH / 1.) DMF, 15 min, 2.) DMF, 0 deg C, 15 min
With
sodium hydroxide; tetrakis(triphenylphosphine) palladium(0); tetrabutyl ammonium fluoride; sodium hydride; triethylamine;
In
tetrahydrofuran; dichloromethane; isopropyl alcohol; benzene;
DOI:10.1021/jm970816j