3-amino-5-N-(3-(3-isopropylureido)benzyl)-2,3-dihydro-5H-1,5-benzoxazepin-4-one

Base Information

Chemical Name:3-amino-5-N-(3-(3-isopropylureido)benzyl)-2,3-dihydro-5H-1,5-benzoxazepin-4-one
CAS No.:239097-88-2
Molecular Formula:C₂₀H₂₄N₄O₃
Molecular Weight:368.436
Hs Code.:

Synonyms:3-amino-5-N-(3-(3-isopropylureido)benzyl)-2,3-dihydro-5H-1,5-benzoxazepin-4-one

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Chemical Property of 3-amino-5-N-(3-(3-isopropylureido)benzyl)-2,3-dihydro-5H-1,5-benzoxazepin-4-one

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Technology Process of 3-amino-5-N-(3-(3-isopropylureido)benzyl)-2,3-dihydro-5H-1,5-benzoxazepin-4-one

There total 6 articles about 3-amino-5-N-(3-(3-isopropylureido)benzyl)-2,3-dihydro-5H-1,5-benzoxazepin-4-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: 80.0%

: 239097-87-1
3-(tert-butoxycarbonylamino)-5-N-(3-(3-isopropylureido)benzyl)-2,3-dihydro-5H-1,5-benzoxazepin-4-one

: 239097-88-2
3-amino-5-N-(3-(3-isopropylureido)benzyl)-2,3-dihydro-5H-1,5-benzoxazepin-4-one

Guidance literature:: With hydrogenchloride; In ethyl acetate; for 0.5h; Ambient temperature;
DOI:10.1021/jm990044m

Reference yield:

: 1877-77-6
3-aminobenzenemethanol

: 239097-88-2
3-amino-5-N-(3-(3-isopropylureido)benzyl)-2,3-dihydro-5H-1,5-benzoxazepin-4-one

Guidance literature:: Multi-step reaction with 5 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: 70 percent / tetra-n-butylammonium bromide, KOH / tetrahydrofuran / 2 h / Ambient temperature

5: 80 percent / HCl / ethyl acetate / 0.5 h / Ambient temperature

With hydrogenchloride; potassium hydroxide; tetrabutylammomium bromide; triethylamine; lithium bromide; In tetrahydrofuran; ethyl acetate; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/jm990044m

Reference yield:

: 211761-74-9
3-(N-(isopropylureido))benzyl bromide

: 239097-88-2
3-amino-5-N-(3-(3-isopropylureido)benzyl)-2,3-dihydro-5H-1,5-benzoxazepin-4-one

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / tetra-n-butylammonium bromide, KOH / tetrahydrofuran / 2 h / Ambient temperature

2: 80 percent / HCl / ethyl acetate / 0.5 h / Ambient temperature

With hydrogenchloride; potassium hydroxide; tetrabutylammomium bromide; In tetrahydrofuran; ethyl acetate;
DOI:10.1021/jm990044m