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

Base Information

Chemical Name:2-(5-cyclohexyl-3-methyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-benzo[f][1,3,5]triazepin-1-yl)-N,N-dimethylacetamide
CAS No.:1384248-85-4
Molecular Formula:C₁₉H₂₆N₄O₃
Molecular Weight:358.44
Hs Code.:

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

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

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

There total 7 articles about 2-(5-cyclohexyl-3-methyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-benzo[f][1,3,5]triazepin-1-yl)-N,N-dimethylacetamide 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: 84.0%

: 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

: 124-40-3
dimethyl amine

: 1384248-85-4
2-(5-cyclohexyl-3-methyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-benzo[f][1,3,5]triazepin-1-yl)-N,N-dimethylacetamide

Guidance literature:: With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; HATU; In N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1016/j.tetlet.2012.05.025

Reference yield:

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

: 1384248-85-4
2-(5-cyclohexyl-3-methyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-benzo[f][1,3,5]triazepin-1-yl)-N,N-dimethylacetamide

Guidance literature:: Multi-step reaction with 5 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: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; HATU / N,N-dimethyl-formamide / 20 °C

With dmap; palladium 10% on activated carbon; hydrogen; sodium hydride; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; HATU; In ethanol; 2,4-dichlorophenoxyacetic acid dimethylamine; ethyl acetate; N,N-dimethyl-formamide; mineral oil;
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

: 1384248-85-4
2-(5-cyclohexyl-3-methyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-benzo[f][1,3,5]triazepin-1-yl)-N,N-dimethylacetamide

Guidance literature:: Multi-step reaction with 2 steps

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

2: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; HATU / N,N-dimethyl-formamide / 20 °C

With dmap; palladium 10% on activated carbon; hydrogen; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; HATU; In ethanol; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1016/j.tetlet.2012.05.025