1-(4-fluorophenyl)ethyl 1-methyl-6-phenyl-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-ylcarbamate

Base Information

Chemical Name:1-(4-fluorophenyl)ethyl 1-methyl-6-phenyl-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-ylcarbamate
CAS No.:1300087-55-1
Molecular Formula:C₂₆H₂₂FN₅O₂
Molecular Weight:455.491
Hs Code.:

Synonyms:1-(4-fluorophenyl)ethyl 1-methyl-6-phenyl-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-ylcarbamate

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Chemical Property of 1-(4-fluorophenyl)ethyl 1-methyl-6-phenyl-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-ylcarbamate

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Technology Process of 1-(4-fluorophenyl)ethyl 1-methyl-6-phenyl-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-ylcarbamate

There total 3 articles about 1-(4-fluorophenyl)ethyl 1-methyl-6-phenyl-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-ylcarbamate 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: 28.0%

: 1300090-37-2
1-(4-fluorophenyl)ethyl 4-nitrophenyl carbonate

: 1-methyl-6-phenyl-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-amine

: 1300087-55-1
1-(4-fluorophenyl)ethyl 1-methyl-6-phenyl-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-ylcarbamate

Guidance literature:: With triethylamine; In acetonitrile; at 75 ℃; for 96h; Inert atmosphere;

Reference yield:

: 403-41-8
1-(4-Fluorophenyl)ethanol

: 1300087-55-1
1-(4-fluorophenyl)ethyl 1-methyl-6-phenyl-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-ylcarbamate

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine / dichloromethane / 48 h / 0 - 20 °C / Inert atmosphere

2: triethylamine / acetonitrile / 96 h / 75 °C / Inert atmosphere

With pyridine; triethylamine; In dichloromethane; acetonitrile;

Reference yield:

: 146135-18-4
phenylmethyl (1-methyl-6-phenyl-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl)carbamate

: 1300087-55-1
1-(4-fluorophenyl)ethyl 1-methyl-6-phenyl-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-ylcarbamate

Guidance literature:: Multi-step reaction with 2 steps

1: cyclohexa-1,4-diene / palladium 10% on activated carbon / methanol / 4 h / 20 °C / Inert atmosphere

2: triethylamine / acetonitrile / 96 h / 75 °C / Inert atmosphere

With cyclohexa-1,4-diene; triethylamine; palladium 10% on activated carbon; In methanol; acetonitrile;