3-((imidazol-1-yl)carbonylamino)-1-N-(3-(N'-(3-isopropylureido))benzyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one

Base Information

Chemical Name:3-((imidazol-1-yl)carbonylamino)-1-N-(3-(N'-(3-isopropylureido))benzyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one
CAS No.:211761-69-2
Molecular Formula:C₂₅H₂₈N₆O₃
Molecular Weight:460.536
Hs Code.:

Synonyms:3-((imidazol-1-yl)carbonylamino)-1-N-(3-(N'-(3-isopropylureido))benzyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 3-((imidazol-1-yl)carbonylamino)-1-N-(3-(N'-(3-isopropylureido))benzyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of 3-((imidazol-1-yl)carbonylamino)-1-N-(3-(N'-(3-isopropylureido))benzyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one

There total 7 articles about 3-((imidazol-1-yl)carbonylamino)-1-N-(3-(N'-(3-isopropylureido))benzyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-2-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: 100.0%

: 530-62-1
1,1'-carbonyldiimidazole

: 211761-68-1
1-[3-(3-amino-2-oxo-2,3,4,5-tetrahydro-benzo[b]azepin-1-ylmethyl)-phenyl]-3-isopropyl-urea

: 211761-69-2
3-((imidazol-1-yl)carbonylamino)-1-N-(3-(N'-(3-isopropylureido))benzyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one

Guidance literature:: In acetonitrile; for 1.5h; Ambient temperature;
DOI:10.1021/jm990044m

Reference yield:

: 1877-77-6
3-aminobenzenemethanol

: 211761-69-2
3-((imidazol-1-yl)carbonylamino)-1-N-(3-(N'-(3-isopropylureido))benzyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one

Guidance literature:: Multi-step reaction with 6 steps

1: 84 percent / acetonitrile / 3 h / 20 - 50 °C

2: 93 percent / Et₃N / dimethylformamide / 1 h / Ambient temperature

3: 80 percent / LiBr / dimethylformamide / 1.3 h / 0 °C

4: tetra-n-butylammonium bromide, KOH / tetrahydrofuran / 2 h / Ambient temperature

5: H₂ / 10 percent Pd/C / methanol / Ambient temperature

6: 100 percent / acetonitrile / 1.5 h / Ambient temperature

With potassium hydroxide; tetrabutylammomium bromide; hydrogen; triethylamine; lithium bromide; palladium on activated charcoal; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/jm990044m

Reference yield:

: 97278-68-7,86499-24-3
3-azido-2,3,4,5-tetrahydro-2-oxo-1 H-1-benzazepine

: 211761-69-2
3-((imidazol-1-yl)carbonylamino)-1-N-(3-(N'-(3-isopropylureido))benzyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: tetra-n-butylammonium bromide, KOH / tetrahydrofuran / 2 h / Ambient temperature

2: H₂ / 10 percent Pd/C / methanol / Ambient temperature

3: 100 percent / acetonitrile / 1.5 h / Ambient temperature

With potassium hydroxide; tetrabutylammomium bromide; hydrogen; palladium on activated charcoal; In tetrahydrofuran; methanol; acetonitrile;
DOI:10.1021/jm990044m