5-{3-[3-(2-aminoethyl)-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl]-1,2,4-oxadiazol-5-yl}-2-[(1-methylethyl)oxy]benzonitrile monohydrochloride

Base Information

Chemical Name:5-{3-[3-(2-aminoethyl)-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl]-1,2,4-oxadiazol-5-yl}-2-[(1-methylethyl)oxy]benzonitrile monohydrochloride
CAS No.:1258855-89-8
Molecular Formula:C₂₄H₂₇N₅O₂*ClH
Molecular Weight:453.972
Hs Code.:

Synonyms:5-{3-[3-(2-aminoethyl)-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl]-1,2,4-oxadiazol-5-yl}-2-[(1-methylethyl)oxy]benzonitrile monohydrochloride

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Chemical Property of 5-{3-[3-(2-aminoethyl)-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl]-1,2,4-oxadiazol-5-yl}-2-[(1-methylethyl)oxy]benzonitrile monohydrochloride

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Technology Process of 5-{3-[3-(2-aminoethyl)-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl]-1,2,4-oxadiazol-5-yl}-2-[(1-methylethyl)oxy]benzonitrile monohydrochloride

There total 8 articles about 5-{3-[3-(2-aminoethyl)-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl]-1,2,4-oxadiazol-5-yl}-2-[(1-methylethyl)oxy]benzonitrile monohydrochloride 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:

: 1258855-90-1
1,1-dimethylethyl {2-[7-(5-{3-cyano-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1,2,4,5-tetrahydro-3H-3-benzazepin-3-yl]ethyl}carbamate

: 1258855-89-8
5-{3-[3-(2-aminoethyl)-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl]-1,2,4-oxadiazol-5-yl}-2-[(1-methylethyl)oxy]benzonitrile monohydrochloride

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; at 20 ℃; for 0.5h;

Reference yield:

: 258273-31-3
3-cyano-4-isopropoxybenzoic acid

: 1258855-89-8
5-{3-[3-(2-aminoethyl)-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl]-1,2,4-oxadiazol-5-yl}-2-[(1-methylethyl)oxy]benzonitrile monohydrochloride

Guidance literature:: Multi-step reaction with 5 steps

1: oxalyl dichloride / N,N-dimethyl-formamide / 4 h / 20 °C

2: pyridine / toluene / 1.5 h / 110 °C / Inert atmosphere; Reflux

3: hydrogenchloride / dichloromethane; 1,4-dioxane; diethyl ether / 3.5 h

4: potassium carbonate / N,N-dimethyl-formamide / 4 h / 45 °C

5: hydrogenchloride / 1,4-dioxane / 0.5 h / 20 °C

With pyridine; hydrogenchloride; oxalyl dichloride; potassium carbonate; N,N-dimethyl-formamide; In 1,4-dioxane; diethyl ether; dichloromethane; N,N-dimethyl-formamide; toluene;

Reference yield:

: 264264-28-0
1,1-dimethylethyl-7-{[(trifluoromethyl)sulfonyl]oxy}-1,2,4,5-tetrahydro-3H-3-benzazepine-3-carboxylate

: 1258855-89-8
5-{3-[3-(2-aminoethyl)-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl]-1,2,4-oxadiazol-5-yl}-2-[(1-methylethyl)oxy]benzonitrile monohydrochloride

Guidance literature:: Multi-step reaction with 6 steps

1: tetrakis(triphenylphosphine) palladium⁽⁰⁾ / N,N-dimethyl-formamide / 1.25 h / 100 °C / Inert atmosphere

2: hydroxylamine hydrochloride; sodium hydrogencarbonate / ethanol / 4 h / 60 °C / Reflux

3: pyridine / toluene / 1.5 h / 110 °C / Inert atmosphere; Reflux

4: hydrogenchloride / dichloromethane; 1,4-dioxane; diethyl ether / 3.5 h

5: potassium carbonate / N,N-dimethyl-formamide / 4 h / 45 °C

6: hydrogenchloride / 1,4-dioxane / 0.5 h / 20 °C

With pyridine; hydrogenchloride; hydroxylamine hydrochloride; sodium hydrogencarbonate; potassium carbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In 1,4-dioxane; diethyl ether; ethanol; dichloromethane; N,N-dimethyl-formamide; toluene;