4-(4-chlorobenzyl)-5-oxo-[1,4]diazepane-1-carboxylic acid t-butyl ester

Base Information

Chemical Name:4-(4-chlorobenzyl)-5-oxo-[1,4]diazepane-1-carboxylic acid t-butyl ester
CAS No.:1076243-01-0
Molecular Formula:C₁₇H₂₃ClN₂O₃
Molecular Weight:338.834
Hs Code.:

Synonyms:4-(4-chlorobenzyl)-5-oxo-[1,4]diazepane-1-carboxylic acid t-butyl ester

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Chemical Property of 4-(4-chlorobenzyl)-5-oxo-[1,4]diazepane-1-carboxylic acid t-butyl ester

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Technology Process of 4-(4-chlorobenzyl)-5-oxo-[1,4]diazepane-1-carboxylic acid t-butyl ester

There total 1 articles about 4-(4-chlorobenzyl)-5-oxo-[1,4]diazepane-1-carboxylic acid t-butyl 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:

Reference yield:

: 622-95-7
4-chlorobenzyl bromide

: 190900-21-1
5-oxo-[1,4]diazepane-1-carboxylic acid tert-butyl ester

: 1076243-01-0
4-(4-chlorobenzyl)-5-oxo-[1,4]diazepane-1-carboxylic acid t-butyl ester

Guidance literature:: 5-oxo-[1,4]diazepane-1-carboxylic acid tert-butyl ester; With potassium hexamethylsilazane; In tetrahydrofuran; at -70 ℃; for 0.25h;

4-chlorobenzyl bromide; In tetrahydrofuran; at -75 ℃; for 6h;

Reference yield:

: 1076243-01-0
4-(4-chlorobenzyl)-5-oxo-[1,4]diazepane-1-carboxylic acid t-butyl ester

: 1076243-02-1
4-(4-chlorobenzyl)-[1,4]diazepan-5-one

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 0 - 20 ℃; for 0.833333h;

Reference yield:

: 1076243-01-0
4-(4-chlorobenzyl)-5-oxo-[1,4]diazepane-1-carboxylic acid t-butyl ester

: 1076242-88-0
N-(2-{3-[4-(4-chlorobenzyl)-5-oxo-[1,4]diazepan-1-yl]-2-hydroxy-propoxy}-4-hydroxyphenyl)-acetamide trifluoroacetate

Guidance literature:: Multi-step reaction with 2 steps

1.1: trifluoroacetic acid / dichloromethane / 0.83 h / 0 - 20 °C

2.1: ethanol / 3.5 h / 80 °C

2.2: 1 h / 50 °C

With trifluoroacetic acid; In ethanol; dichloromethane;