4-((10-ethyl-10H-phenothiazin-3-yl)methyleneamino)-1,5-dimethyl-2-phenyl-1H-pyrazol-3(2H)-one

Base Information

• Chemical Name: 4-((10-ethyl-10H-phenothiazin-3-yl)methyleneamino)-1,5-dimethyl-2-phenyl-1H-pyrazol-3(2H)-one
• CAS No.: 1417521-51-7
• Molecular Formula: C₂₆H₂₄N₄OS
• Molecular Weight: 440.569
• Mol file: 1417521-51-7.mol

Synonyms:4-((10-ethyl-10H-phenothiazin-3-yl)methyleneamino)-1,5-dimethyl-2-phenyl-1H-pyrazol-3(2H)-one

Chemical Property of 4-((10-ethyl-10H-phenothiazin-3-yl)methyleneamino)-1,5-dimethyl-2-phenyl-1H-pyrazol-3(2H)-one

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 4-((10-ethyl-10H-phenothiazin-3-yl)methyleneamino)-1,5-dimethyl-2-phenyl-1H-pyrazol-3(2H)-one

There total 3 articles about 4-((10-ethyl-10H-phenothiazin-3-yl)methyleneamino)-1,5-dimethyl-2-phenyl-1H-pyrazol-3(2H)-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: 86.0%

10-ethyl-10H-phenothiazine-3-carbaldehyde (18413-61-1) + 4-amino-2,3-dimethyl-1-phenylpyrazolin-5-one (83-07-8) → 4-((10-ethyl-10H-phenothiazin-3-yl)methyleneamino)-1,5-dimethyl-2-phenyl-1H-pyrazol-3(2H)-one (1417521-51-7)

Guidance literature:

In ethanol; at 70 ℃; Inert atmosphere;

DOI:10.1002/poc.2948

Reference yield:

10-ethyl-phenothiazine (1637-16-7) → 4-((10-ethyl-10H-phenothiazin-3-yl)methyleneamino)-1,5-dimethyl-2-phenyl-1H-pyrazol-3(2H)-one (1417521-51-7)

Guidance literature:

Multi-step reaction with 2 steps

1: trichlorophosphate / chloroform / 100 °C / Cooling with ice; Inert atmosphere

2: ethanol / 70 °C / Inert atmosphere

With trichlorophosphate; In ethanol; chloroform; 1: |Vilsmeier-Haack Formylation / 2: |Schiff Reaction;

DOI:10.1002/poc.2948

Reference yield:

10H-phenothiazine (92-84-2) → 4-((10-ethyl-10H-phenothiazin-3-yl)methyleneamino)-1,5-dimethyl-2-phenyl-1H-pyrazol-3(2H)-one (1417521-51-7)

Guidance literature:

Multi-step reaction with 3 steps

1.1: sodium hydroxide / dimethyl sulfoxide / 1 h / Inert atmosphere

1.2: 3 h / 20 °C / Inert atmosphere

2.1: trichlorophosphate / chloroform / 100 °C / Cooling with ice; Inert atmosphere

3.1: ethanol / 70 °C / Inert atmosphere

With sodium hydroxide; trichlorophosphate; In ethanol; chloroform; dimethyl sulfoxide; 2.1: |Vilsmeier-Haack Formylation / 3.1: |Schiff Reaction;

DOI:10.1002/poc.2948

upstream raw materials:

10-ethyl-phenothiazine

10H-phenothiazine

10-ethyl-10H-phenothiazine-3-carbaldehyde

4-amino-2,3-dimethyl-1-phenylpyrazolin-5-one