N-[4-(2-oxo-2-{(2E)-2-[2-oxo-1-(piperidin-1-ylmethyl)-1,2-dihydro-3H-indol-3-ylidene]hydrazinyl}ethoxy)phenyl]acetamide

Base Information

• Chemical Name: N-[4-(2-oxo-2-{(2E)-2-[2-oxo-1-(piperidin-1-ylmethyl)-1,2-dihydro-3H-indol-3-ylidene]hydrazinyl}ethoxy)phenyl]acetamide
• CAS No.: 81820-04-4
• Molecular Formula: C₂₄H₂₇N₅O₄
• Molecular Weight: 449.509
• Mol file: 81820-04-4.mol

Synonyms:

Chemical Property of N-[4-(2-oxo-2-{(2E)-2-[2-oxo-1-(piperidin-1-ylmethyl)-1,2-dihydro-3H-indol-3-ylidene]hydrazinyl}ethoxy)phenyl]acetamide

Chemical Property:

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Density: 1.33g/cm³

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of N-[4-(2-oxo-2-{(2E)-2-[2-oxo-1-(piperidin-1-ylmethyl)-1,2-dihydro-3H-indol-3-ylidene]hydrazinyl}ethoxy)phenyl]acetamide

There total 3 articles about N-[4-(2-oxo-2-{(2E)-2-[2-oxo-1-(piperidin-1-ylmethyl)-1,2-dihydro-3H-indol-3-ylidene]hydrazinyl}ethoxy)phenyl]acetamide 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:

indole-2,3-dione (91-56-5,1186480-61-4,84788-92-1) → N-{4-[2-Oxo-1-piperidin-1-ylmethyl-1,2-dihydro-indol-(3Z)-ylidene-hydrazinocarbonylmethoxy]-phenyl}-acetamide (81820-04-4)

Guidance literature:

Multi-step reaction with 2 steps

1: 96 percent / acetic acid / ethanol / 4 h / Heating

2: 1.) ethanol, water, heating, 2.) room temperature

With acetic acid; In ethanol;

Reference yield:

N‐(4‐(2‐hydrazinyl‐2‐oxoethoxy)phenyl) acetamide (75129-75-8) → N-{4-[2-Oxo-1-piperidin-1-ylmethyl-1,2-dihydro-indol-(3Z)-ylidene-hydrazinocarbonylmethoxy]-phenyl}-acetamide (81820-04-4)

Guidance literature:

Multi-step reaction with 2 steps

1: 96 percent / acetic acid / ethanol / 4 h / Heating

2: 1.) ethanol, water, heating, 2.) room temperature

With acetic acid; In ethanol;

Reference yield:

piperidine (110-89-4) + formaldehyd (50-00-0,30525-89-4,61233-19-0) + 3-(4'-acetamidophenoxyacetylhydrazono)indolin-2-one (81820-16-8) → N-{4-[2-Oxo-1-piperidin-1-ylmethyl-1,2-dihydro-indol-(3Z)-ylidene-hydrazinocarbonylmethoxy]-phenyl}-acetamide (81820-04-4)

Guidance literature:

Multistep reaction; 1.) ethanol, water, heating, 2.) room temperature;

upstream raw materials:

piperidine

formaldehyd

3-(4'-acetamidophenoxyacetylhydrazono)indolin-2-one

indole-2,3-dione