3-amino-5-(2,6-dichlorophenyl)-1-(4-methoxybenzyl)-1H-benzo[e] [1,4]diazepin-2(3H)-one

Base Information

Chemical Name:3-amino-5-(2,6-dichlorophenyl)-1-(4-methoxybenzyl)-1H-benzo[e] [1,4]diazepin-2(3H)-one
CAS No.:1271523-29-5
Molecular Formula:C₂₃H₁₉Cl₂N₃O₂
Molecular Weight:440.329
Hs Code.:

Synonyms:3-amino-5-(2,6-dichlorophenyl)-1-(4-methoxybenzyl)-1H-benzo[e] [1,4]diazepin-2(3H)-one

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Chemical Property of 3-amino-5-(2,6-dichlorophenyl)-1-(4-methoxybenzyl)-1H-benzo[e] [1,4]diazepin-2(3H)-one

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Technology Process of 3-amino-5-(2,6-dichlorophenyl)-1-(4-methoxybenzyl)-1H-benzo[e] [1,4]diazepin-2(3H)-one

There total 9 articles about 3-amino-5-(2,6-dichlorophenyl)-1-(4-methoxybenzyl)-1H-benzo[e] [1,4]diazepin-2(3H)-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:

: 1271523-25-1
tert-butyl 5-(2,6-dichlorophenyl)-1-(4-methoxybenzyl)-2-oxo-2,3-dihydro-1H-benzo[e] [1,4]diazepin-3-ylcarbamate

: 1271523-29-5
3-amino-5-(2,6-dichlorophenyl)-1-(4-methoxybenzyl)-1H-benzo[e] [1,4]diazepin-2(3H)-one

Guidance literature:: With trifluoroacetic acid; In dichloromethane; for 3h;

Reference yield:

: 118-92-3,159201-01-1,50816-84-7,80206-34-4,104809-47-4
anthranilic acid

: 1271523-29-5
3-amino-5-(2,6-dichlorophenyl)-1-(4-methoxybenzyl)-1H-benzo[e] [1,4]diazepin-2(3H)-one

Guidance literature:: Multi-step reaction with 8 steps

1.1: acetic acid / dichloromethane / 2 h / 20 °C

1.2: 0 - 20 °C

2.1: bis(trichloromethyl) carbonate / tetrahydrofuran / 20 °C

3.1: acetic acid / Reflux

4.1: trichlorophosphate; N,N-dimethyl-aniline / toluene / Reflux

5.1: potassium tert-butylate / tetrahydrofuran / 0.5 h / -78 °C / Inert atmosphere

5.2: 0.75 h / -78 °C / Inert atmosphere

5.3: -78 - 20 °C / Inert atmosphere

6.1: hydrogen / platinum(IV) oxide / 1,4-dioxane

7.1: potassium carbonate; silver carbonate / tetrahydrofuran / 1 h / Reflux

8.1: trifluoroacetic acid / dichloromethane / 3 h

With bis(trichloromethyl) carbonate; potassium tert-butylate; hydrogen; potassium carbonate; acetic acid; N,N-dimethyl-aniline; silver carbonate; trifluoroacetic acid; trichlorophosphate; platinum(IV) oxide; In tetrahydrofuran; 1,4-dioxane; dichloromethane; acetic acid; toluene;

Reference yield:

: 16512-74-6
1-(4-methoxybenzyl)-2H-benzo[d][1,3]oxazine-2,4(1H)-dione

: 1271523-29-5
3-amino-5-(2,6-dichlorophenyl)-1-(4-methoxybenzyl)-1H-benzo[e] [1,4]diazepin-2(3H)-one

Guidance literature:: Multi-step reaction with 6 steps

1.1: acetic acid / Reflux

2.1: trichlorophosphate; N,N-dimethyl-aniline / toluene / Reflux

3.1: potassium tert-butylate / tetrahydrofuran / 0.5 h / -78 °C / Inert atmosphere

3.2: 0.75 h / -78 °C / Inert atmosphere

3.3: -78 - 20 °C / Inert atmosphere

4.1: hydrogen / platinum(IV) oxide / 1,4-dioxane

5.1: potassium carbonate; silver carbonate / tetrahydrofuran / 1 h / Reflux

6.1: trifluoroacetic acid / dichloromethane / 3 h

With potassium tert-butylate; hydrogen; potassium carbonate; N,N-dimethyl-aniline; silver carbonate; trifluoroacetic acid; trichlorophosphate; platinum(IV) oxide; In tetrahydrofuran; 1,4-dioxane; dichloromethane; acetic acid; toluene;