Technology Process of ethyl N6-[N-(methoxycarbonyl)-β-phenyl-L-phenylalanyl]-4,4-difluoro-N2-[(4-nitrophenyl)sulfonyl]-L-lysinate
There total 8 articles about ethyl N6-[N-(methoxycarbonyl)-β-phenyl-L-phenylalanyl]-4,4-difluoro-N2-[(4-nitrophenyl)sulfonyl]-L-lysinate 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 9 steps
1.1: triethylamine / dmap / acetonitrile / 20 °C
2.1: dmap / acetonitrile / 48 h / 20 °C
3.1: diisobutylaluminium hydride / toluene; diethyl ether / 0.75 h / -70 °C
3.2: 1.5 h / 20 °C
4.1: N-fluorobis(benzenesulfon)imide; rac-Pro-OH / isopropyl alcohol; tetrahydrofuran / 24 h / 20 °C
4.2: 0 - 20 °C
4.3: 3 h / 0 - 20 °C
5.1: water; sodium tetrahydroborate / tetrahydrofuran / 4 h / 20 °C
6.1: hydrogen / palladium 10% on activated carbon / ethyl acetate; ethanol / 20 h / 1810.07 Torr
7.1: sodium hydrogencarbonate / water; tetrahydrofuran / 0 - 20 °C
8.1: trifluoroacetic acid; methoxybenzene / dichloromethane / 2 h / 0 - 20 °C
9.1: pyridine / dmap / 85 °C
With
pyridine; sodium tetrahydroborate; water; hydrogen; diisobutylaluminium hydride; sodium hydrogencarbonate; methoxybenzene; N-fluorobis(benzenesulfon)imide; triethylamine; trifluoroacetic acid; rac-Pro-OH;
dmap; palladium 10% on activated carbon;
In
tetrahydrofuran; diethyl ether; ethanol; dichloromethane; water; ethyl acetate; isopropyl alcohol; toluene; acetonitrile;
- Guidance literature:
-
Multi-step reaction with 7 steps
1.1: diisobutylaluminium hydride / toluene; diethyl ether / 0.75 h / -70 °C
1.2: 1.5 h / 20 °C
2.1: N-fluorobis(benzenesulfon)imide; rac-Pro-OH / isopropyl alcohol; tetrahydrofuran / 24 h / 20 °C
2.2: 0 - 20 °C
2.3: 3 h / 0 - 20 °C
3.1: water; sodium tetrahydroborate / tetrahydrofuran / 4 h / 20 °C
4.1: hydrogen / palladium 10% on activated carbon / ethyl acetate; ethanol / 20 h / 1810.07 Torr
5.1: sodium hydrogencarbonate / water; tetrahydrofuran / 0 - 20 °C
6.1: trifluoroacetic acid; methoxybenzene / dichloromethane / 2 h / 0 - 20 °C
7.1: pyridine / dmap / 85 °C
With
pyridine; sodium tetrahydroborate; water; hydrogen; diisobutylaluminium hydride; sodium hydrogencarbonate; methoxybenzene; N-fluorobis(benzenesulfon)imide; trifluoroacetic acid; rac-Pro-OH;
dmap; palladium 10% on activated carbon;
In
tetrahydrofuran; diethyl ether; ethanol; dichloromethane; water; ethyl acetate; isopropyl alcohol; toluene;
- Guidance literature:
-
Multi-step reaction with 8 steps
1.1: dmap / acetonitrile / 48 h / 20 °C
2.1: diisobutylaluminium hydride / toluene; diethyl ether / 0.75 h / -70 °C
2.2: 1.5 h / 20 °C
3.1: N-fluorobis(benzenesulfon)imide; rac-Pro-OH / isopropyl alcohol; tetrahydrofuran / 24 h / 20 °C
3.2: 0 - 20 °C
3.3: 3 h / 0 - 20 °C
4.1: water; sodium tetrahydroborate / tetrahydrofuran / 4 h / 20 °C
5.1: hydrogen / palladium 10% on activated carbon / ethyl acetate; ethanol / 20 h / 1810.07 Torr
6.1: sodium hydrogencarbonate / water; tetrahydrofuran / 0 - 20 °C
7.1: trifluoroacetic acid; methoxybenzene / dichloromethane / 2 h / 0 - 20 °C
8.1: pyridine / dmap / 85 °C
With
pyridine; sodium tetrahydroborate; water; hydrogen; diisobutylaluminium hydride; sodium hydrogencarbonate; methoxybenzene; N-fluorobis(benzenesulfon)imide; trifluoroacetic acid; rac-Pro-OH;
dmap; palladium 10% on activated carbon;
In
tetrahydrofuran; diethyl ether; ethanol; dichloromethane; water; ethyl acetate; isopropyl alcohol; toluene; acetonitrile;