(E)-(5-chloro-2-{3-[3-(4-fluorobenzyl)-3,8-diazabicyclo[3.2.1]oct-8-yl]-3-oxopropenyl}-4-methoxyphenyl)-urea

Base Information

Chemical Name:(E)-(5-chloro-2-{3-[3-(4-fluorobenzyl)-3,8-diazabicyclo[3.2.1]oct-8-yl]-3-oxopropenyl}-4-methoxyphenyl)-urea
CAS No.:868406-59-1
Molecular Formula:C₂₄H₂₆ClFN₄O₃
Molecular Weight:472.947
Hs Code.:

Synonyms:(E)-(5-chloro-2-{3-[3-(4-fluorobenzyl)-3,8-diazabicyclo[3.2.1]oct-8-yl]-3-oxopropenyl}-4-methoxyphenyl)-urea

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Chemical Property of (E)-(5-chloro-2-{3-[3-(4-fluorobenzyl)-3,8-diazabicyclo[3.2.1]oct-8-yl]-3-oxopropenyl}-4-methoxyphenyl)-urea

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Technology Process of (E)-(5-chloro-2-{3-[3-(4-fluorobenzyl)-3,8-diazabicyclo[3.2.1]oct-8-yl]-3-oxopropenyl}-4-methoxyphenyl)-urea

There total 8 articles about (E)-(5-chloro-2-{3-[3-(4-fluorobenzyl)-3,8-diazabicyclo[3.2.1]oct-8-yl]-3-oxopropenyl}-4-methoxyphenyl)-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: 69.0%

: 868406-58-0
(E)-3-(2-amino-4-chloro-5-methoxyphenyl)-1-[3-(4-fluorobenzyl)-3,8-diazabicyclo[3.2.1]oct-8-yl]-propenone

: 917-61-3
sodium isocyanate

: 868406-59-1
(E)-(5-chloro-2-{3-[3-(4-fluorobenzyl)-3,8-diazabicyclo[3.2.1]oct-8-yl]-3-oxopropenyl}-4-methoxyphenyl)-urea

Guidance literature:: (E)-3-(2-amino-4-chloro-5-methoxyphenyl)-1-[3-(4-fluorobenzyl)-3,8-diazabicyclo[3.2.1]oct-8-yl]-propenone; sodium isocyanate; With acetic acid; In water; at 20 ℃; for 0.583333h;

With sodium carbonate; In water;

Reference yield:

: 685536-12-3
2-bromo-5-chloro-4-methoxy-phenylamine

: 868406-59-1
(E)-(5-chloro-2-{3-[3-(4-fluorobenzyl)-3,8-diazabicyclo[3.2.1]oct-8-yl]-3-oxopropenyl}-4-methoxyphenyl)-urea

Guidance literature:: Multi-step reaction with 4 steps

1: bis-triphenylphosphine-palladium(II) chloride / DMF (N,N-dimethyl-formamide) / 0.33 h / 140 °C

2: sodium hydroxide; ethanol; water / 0.17 h / Heating / reflux

3: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / DMF (N,N-dimethyl-formamide) / 20 °C

4: acetic acid / water / 0.58 h / 20 °C

With sodium hydroxide; ethanol; water; benzotriazol-1-ol; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; bis-triphenylphosphine-palladium(II) chloride; In DMF (N,N-dimethyl-formamide); water;

Reference yield:

: 5345-54-0
3-chloro-4-methoxyaniline

: 868406-59-1
(E)-(5-chloro-2-{3-[3-(4-fluorobenzyl)-3,8-diazabicyclo[3.2.1]oct-8-yl]-3-oxopropenyl}-4-methoxyphenyl)-urea

Guidance literature:: Multi-step reaction with 5 steps

1: N-Bromosuccinimide / dichloromethane / 0.08 h

2: bis-triphenylphosphine-palladium(II) chloride / DMF (N,N-dimethyl-formamide) / 0.33 h / 140 °C

3: sodium hydroxide; ethanol; water / 0.17 h / Heating / reflux

4: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / DMF (N,N-dimethyl-formamide) / 20 °C

5: acetic acid / water / 0.58 h / 20 °C

With sodium hydroxide; N-Bromosuccinimide; ethanol; water; benzotriazol-1-ol; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; bis-triphenylphosphine-palladium(II) chloride; In DMF (N,N-dimethyl-formamide); dichloromethane; water;