8-(2,6-dichlorobenzyl)-6-{[2-methoxy-4-(piperazin-1-yl)phenyl]amino}-1,2,3,4-tetrahydro-5H-pyrido[2,3-e][1,4]diazepin-5-one

Base Information

Chemical Name:8-(2,6-dichlorobenzyl)-6-{[2-methoxy-4-(piperazin-1-yl)phenyl]amino}-1,2,3,4-tetrahydro-5H-pyrido[2,3-e][1,4]diazepin-5-one
CAS No.:1390655-14-7
Molecular Formula:C₂₆H₂₈Cl₂N₆O₂
Molecular Weight:527.453
Hs Code.:

Synonyms:8-(2,6-dichlorobenzyl)-6-{[2-methoxy-4-(piperazin-1-yl)phenyl]amino}-1,2,3,4-tetrahydro-5H-pyrido[2,3-e][1,4]diazepin-5-one

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Chemical Property of 8-(2,6-dichlorobenzyl)-6-{[2-methoxy-4-(piperazin-1-yl)phenyl]amino}-1,2,3,4-tetrahydro-5H-pyrido[2,3-e][1,4]diazepin-5-one

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Technology Process of 8-(2,6-dichlorobenzyl)-6-{[2-methoxy-4-(piperazin-1-yl)phenyl]amino}-1,2,3,4-tetrahydro-5H-pyrido[2,3-e][1,4]diazepin-5-one

There total 13 articles about 8-(2,6-dichlorobenzyl)-6-{[2-methoxy-4-(piperazin-1-yl)phenyl]amino}-1,2,3,4-tetrahydro-5H-pyrido[2,3-e][1,4]diazepin-5-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:

: 1390656-56-0
tert-butyl 4-(4-(8-chloro-5-oxo-2,3,4,5-tetrahydro-1H-pyrido[2,3-e][1,4]diazepin-6-ylamino)-3-methoxyphenyl)piperazine-1-carboxylate

: 117269-75-7
(2,6-dichlorobenzyl)zinc(II) bromide

: 1390655-14-7
8-(2,6-dichlorobenzyl)-6-{[2-methoxy-4-(piperazin-1-yl)phenyl]amino}-1,2,3,4-tetrahydro-5H-pyrido[2,3-e][1,4]diazepin-5-one

Guidance literature:: tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; at 120 ℃; for 1h; Microwave irradiation;

Reference yield:

: 16063-69-7
2,4,6-trichloropyridine

: 1390655-14-7
8-(2,6-dichlorobenzyl)-6-{[2-methoxy-4-(piperazin-1-yl)phenyl]amino}-1,2,3,4-tetrahydro-5H-pyrido[2,3-e][1,4]diazepin-5-one

Guidance literature:: Multi-step reaction with 7 steps

1.1: diisopropylamine; n-butyllithium / hexane; tetrahydrofuran / 1.5 h

1.2: 1 h / 20 °C

2.1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 2.5 h / 0 °C

3.1: triethylamine / dichloromethane / 3 h / 0 °C

4.1: trifluoroacetic acid / dichloromethane / 20 °C

5.1: triethylamine; cesium fluoride / N,N-dimethyl-formamide / 12 h / 75 °C / Inert atmosphere

6.1: N-ethyl-N,N-diisopropylamine / 1,4-dioxane / 48 h / 120 °C / Sealed tube

7.1: tetrakis(triphenylphosphine) palladium⁽⁰⁾ / tetrahydrofuran / 1 h / 120 °C / Microwave irradiation

With n-butyllithium; oxalyl dichloride; triethylamine; diisopropylamine; N-ethyl-N,N-diisopropylamine; cesium fluoride; trifluoroacetic acid; tetrakis(triphenylphosphine) palladium⁽⁰⁾; N,N-dimethyl-formamide; In tetrahydrofuran; 1,4-dioxane; hexane; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 69422-72-6
2,4,6-trichloronicotinoic acid

: 1390655-14-7
8-(2,6-dichlorobenzyl)-6-{[2-methoxy-4-(piperazin-1-yl)phenyl]amino}-1,2,3,4-tetrahydro-5H-pyrido[2,3-e][1,4]diazepin-5-one

Guidance literature:: Multi-step reaction with 6 steps

1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 2.5 h / 0 °C

2: triethylamine / dichloromethane / 3 h / 0 °C

3: trifluoroacetic acid / dichloromethane / 20 °C

4: triethylamine; cesium fluoride / N,N-dimethyl-formamide / 12 h / 75 °C / Inert atmosphere

5: N-ethyl-N,N-diisopropylamine / 1,4-dioxane / 48 h / 120 °C / Sealed tube

6: tetrakis(triphenylphosphine) palladium⁽⁰⁾ / tetrahydrofuran / 1 h / 120 °C / Microwave irradiation

With oxalyl dichloride; triethylamine; N-ethyl-N,N-diisopropylamine; cesium fluoride; trifluoroacetic acid; tetrakis(triphenylphosphine) palladium⁽⁰⁾; N,N-dimethyl-formamide; In tetrahydrofuran; 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide;