N-sec-butyl-2-(5-cyclohexyl-3-methyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-benzo[f][1,3,5]triazepin-1-yl)acetamide

Base Information

Chemical Name:N-sec-butyl-2-(5-cyclohexyl-3-methyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-benzo[f][1,3,5]triazepin-1-yl)acetamide
CAS No.:1384248-83-2
Molecular Formula:C₂₁H₃₀N₄O₃
Molecular Weight:386.494
Hs Code.:

Synonyms:N-sec-butyl-2-(5-cyclohexyl-3-methyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-benzo[f][1,3,5]triazepin-1-yl)acetamide

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Chemical Property of N-sec-butyl-2-(5-cyclohexyl-3-methyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-benzo[f][1,3,5]triazepin-1-yl)acetamide

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Technology Process of N-sec-butyl-2-(5-cyclohexyl-3-methyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-benzo[f][1,3,5]triazepin-1-yl)acetamide

There total 7 articles about N-sec-butyl-2-(5-cyclohexyl-3-methyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-benzo[f][1,3,5]triazepin-1-yl)acetamide 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:

: 74628-31-2
N-1-cyclohexylbenzene-1,2-diamine

: 1384248-83-2
N-sec-butyl-2-(5-cyclohexyl-3-methyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-benzo[f][1,3,5]triazepin-1-yl)acetamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 7 h / 65 °C

2.1: 2,4-dichlorophenoxyacetic acid dimethylamine / 0.5 h / 150 °C / Microwave irradiation

3.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 20 °C

3.2: 16 h

4.1: palladium 10% on activated carbon; hydrogen / ethanol; ethyl acetate / 20 °C

5.1: thionyl chloride; N,N-dimethyl-formamide / dichloromethane / 1 h / 20 °C

6.1: triethylamine / dichloromethane / 20 °C

With thionyl chloride; palladium 10% on activated carbon; hydrogen; sodium hydride; potassium carbonate; triethylamine; N,N-dimethyl-formamide; In ethanol; dichloromethane; 2,4-dichlorophenoxyacetic acid dimethylamine; ethyl acetate; N,N-dimethyl-formamide; mineral oil;
DOI:10.1016/j.tetlet.2012.05.025

Reference yield:

: 1384248-75-2
2-(5-cyclohexyl-3-methyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-benzo[f][1,3,5]triazepin-1-yl)acetic acid

: 1384248-83-2
N-sec-butyl-2-(5-cyclohexyl-3-methyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-benzo[f][1,3,5]triazepin-1-yl)acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride; N,N-dimethyl-formamide / dichloromethane / 1 h / 20 °C

2: triethylamine / dichloromethane / 20 °C

With thionyl chloride; triethylamine; N,N-dimethyl-formamide; In dichloromethane;
DOI:10.1016/j.tetlet.2012.05.025

Reference yield:

: 1384248-64-9
benzyl 2-(5-cyclohexyl-3-methyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-benzo[f][1,3,5]triazepin-1-yl)acetate

: 1384248-83-2
N-sec-butyl-2-(5-cyclohexyl-3-methyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-benzo[f][1,3,5]triazepin-1-yl)acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: palladium 10% on activated carbon; hydrogen / ethanol; ethyl acetate / 20 °C

2: thionyl chloride; N,N-dimethyl-formamide / dichloromethane / 1 h / 20 °C

3: triethylamine / dichloromethane / 20 °C

With thionyl chloride; palladium 10% on activated carbon; hydrogen; triethylamine; N,N-dimethyl-formamide; In ethanol; dichloromethane; ethyl acetate;
DOI:10.1016/j.tetlet.2012.05.025