5,11-dihydro-11-({4-[p-({[2-(Boc-amino)ethyl]amino}carbonyl)benzyl]-1-piperazinyl}acetyl)-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one

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Chemical Name:5,11-dihydro-11-({4-[p-({[2-(Boc-amino)ethyl]amino}carbonyl)benzyl]-1-piperazinyl}acetyl)-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one
CAS No.:133727-68-1
Molecular Formula:C₃₃H₃₉N₇O₅
Molecular Weight:613.717
Hs Code.:

Synonyms:5,11-dihydro-11-({4-[p-({[2-(Boc-amino)ethyl]amino}carbonyl)benzyl]-1-piperazinyl}acetyl)-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one

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Chemical Property of 5,11-dihydro-11-({4-[p-({[2-(Boc-amino)ethyl]amino}carbonyl)benzyl]-1-piperazinyl}acetyl)-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one

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Technology Process of 5,11-dihydro-11-({4-[p-({[2-(Boc-amino)ethyl]amino}carbonyl)benzyl]-1-piperazinyl}acetyl)-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one

There total 4 articles about 5,11-dihydro-11-({4-[p-({[2-(Boc-amino)ethyl]amino}carbonyl)benzyl]-1-piperazinyl}acetyl)-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one 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: 72.0%

: 120131-81-9
p-(bromomethyl)-N-<2-(Boc-amino)ethyl>benzamide

: 63257-31-8,122859-63-6
N-Demethyl-Pirenzepin

: 133727-68-1
5,11-dihydro-11-({4-[p-({[2-(Boc-amino)ethyl]amino}carbonyl)benzyl]-1-piperazinyl}acetyl)-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one

Guidance literature:: With triethylamine; In tetrahydrofuran; methanol; at 25 - 40 ℃;
DOI:10.1021/jm00111a032

Reference yield:

: 29868-97-1,93173-05-8
pirenzepine dihydrochloride

: 133727-68-1
5,11-dihydro-11-({4-[p-({[2-(Boc-amino)ethyl]amino}carbonyl)benzyl]-1-piperazinyl}acetyl)-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) α-chloroethyl chloroformate, N,N,N-diisopropylethylamine, 2.) 1 M HCl in ether / 1.) chloroform, reflux, 1 h, 2.) methanol, reflux, 3 h

2: 72 percent / triethylamine / tetrahydrofuran; methanol / 25 - 40 °C

With hydrogenchloride; carbonochloridic acid 1-chloro-ethyl ester; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol;
DOI:10.1021/jm00111a032

Reference yield:

: 28797-48-0
11-(chloroacetyl)-5,11-dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one

: 133727-68-1
5,11-dihydro-11-({4-[p-({[2-(Boc-amino)ethyl]amino}carbonyl)benzyl]-1-piperazinyl}acetyl)-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one

Guidance literature:: Multi-step reaction with 2 steps

1: dioxane / 1 h / Heating

2: 72 percent / triethylamine / tetrahydrofuran; methanol / 25 - 40 °C

With triethylamine; In tetrahydrofuran; 1,4-dioxane; methanol;
DOI:10.1021/jm00111a032