1-(4-fluorobenzylidene)-3-(1-(morpholinomethyl)-2,3-dioxoindolin-5-yl)urea

Base Information

• Chemical Name: 1-(4-fluorobenzylidene)-3-(1-(morpholinomethyl)-2,3-dioxoindolin-5-yl)urea
• CAS No.: 1347605-72-4
• Molecular Formula: C₂₁H₁₉FN₄O₄
• Molecular Weight: 410.405
• Mol file: 1347605-72-4.mol

Synonyms:1-(4-fluorobenzylidene)-3-(1-(morpholinomethyl)-2,3-dioxoindolin-5-yl)urea

Chemical Property of 1-(4-fluorobenzylidene)-3-(1-(morpholinomethyl)-2,3-dioxoindolin-5-yl)urea

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 1-(4-fluorobenzylidene)-3-(1-(morpholinomethyl)-2,3-dioxoindolin-5-yl)urea

There total 5 articles about 1-(4-fluorobenzylidene)-3-(1-(morpholinomethyl)-2,3-dioxoindolin-5-yl)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: 66.0%

1-(1-(morpholinomethyl)-2,3-dioxoindolin-5-yl)urea (1347606-00-1) + 4-fluorobenzaldehyde (459-57-4) → 1-(4-fluorobenzylidene)-3-(1-(morpholinomethyl)-2,3-dioxoindolin-5-yl)urea (1347605-72-4)

Guidance literature:

With acetic acid; In ethanol; for 8h; Reflux;

DOI:10.1016/j.ejmech.2011.10.020

Reference yield:

1-(morpholinomethyl)-5-amino indoline-2,3-dione (1347605-95-1) → 1-(4-fluorobenzylidene)-3-(1-(morpholinomethyl)-2,3-dioxoindolin-5-yl)urea (1347605-72-4)

Guidance literature:

Multi-step reaction with 2 steps

1: acetic acid / water / 0.5 h

2: acetic acid / ethanol / 8 h / Reflux

With acetic acid; In ethanol; water;

DOI:10.1016/j.ejmech.2011.10.020

Reference yield:

5-nitroisatin (611-09-6) → 1-(4-fluorobenzylidene)-3-(1-(morpholinomethyl)-2,3-dioxoindolin-5-yl)urea (1347605-72-4)

Guidance literature:

Multi-step reaction with 4 steps

1: ethanol / 3 h / 20 °C

2: hydrogenchloride; iron / ethanol; water / 4 h / 80 - 85 °C

3: acetic acid / water / 0.5 h

4: acetic acid / ethanol / 8 h / Reflux

With hydrogenchloride; iron; acetic acid; In ethanol; water; 1: Mannich reaction;

DOI:10.1016/j.ejmech.2011.10.020

upstream raw materials:

1-(morpholinomethyl)-5-nitroindoline-2,3-dione

1-(morpholinomethyl)-5-amino indoline-2,3-dione

1-(1-(morpholinomethyl)-2,3-dioxoindolin-5-yl)urea

4-fluorobenzaldehyde