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

Base Information

Chemical Name:1-[3-(3-azido-2-oxo-2,3,4,5-tetrahydro-benzo[b]azepin-1-ylmethyl)-phenyl]-3-isopropyl-urea
CAS No.:211761-67-0
Molecular Formula:C₂₁H₂₄N₆O₂
Molecular Weight:392.461
Hs Code.:

1-[3-(3-azido-2-oxo-2,3,4,5-tetrahydro-benzo[<i>b</i>]azepin-1-ylmethyl)-phenyl]-3-isopropyl-urea

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

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Chemical Property of 1-[3-(3-azido-2-oxo-2,3,4,5-tetrahydro-benzo[b]azepin-1-ylmethyl)-phenyl]-3-isopropyl-urea

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Technology Process of 1-[3-(3-azido-2-oxo-2,3,4,5-tetrahydro-benzo[b]azepin-1-ylmethyl)-phenyl]-3-isopropyl-urea

There total 4 articles about 1-[3-(3-azido-2-oxo-2,3,4,5-tetrahydro-benzo[b]azepin-1-ylmethyl)-phenyl]-3-isopropyl-urea 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:

: 1877-77-6
3-aminobenzenemethanol

: 211761-67-0
1-[3-(3-azido-2-oxo-2,3,4,5-tetrahydro-benzo[b]azepin-1-ylmethyl)-phenyl]-3-isopropyl-urea

Guidance literature:: Multi-step reaction with 4 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

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

Reference yield:

: 211761-72-7
3-(N-(isopropylureido))benzyl alcohol

: 211761-67-0
1-[3-(3-azido-2-oxo-2,3,4,5-tetrahydro-benzo[b]azepin-1-ylmethyl)-phenyl]-3-isopropyl-urea

Guidance literature:: Multi-step reaction with 3 steps

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

2: 80 percent / LiBr / dimethylformamide / 1.3 h / 0 °C

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

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

Reference yield:

: 211761-73-8
methanesulfonic acid 3-(3-isopropyl-ureido)-benzyl ester

: 211761-67-0
1-[3-(3-azido-2-oxo-2,3,4,5-tetrahydro-benzo[b]azepin-1-ylmethyl)-phenyl]-3-isopropyl-urea

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / LiBr / dimethylformamide / 1.3 h / 0 °C

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

With potassium hydroxide; tetrabutylammomium bromide; lithium bromide; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1021/jm990044m