5-amino-6-(4-methoxyphenyl)pyridazin-3(2H)-one

Base Information

• Chemical Name: 5-amino-6-(4-methoxyphenyl)pyridazin-3(2H)-one
• CAS No.: 220967-27-1
• Molecular Formula: C11H11N3O2
• Molecular Weight: 217.22
• DSSTox Substance ID: DTXSID60440367
• Nikkaji Number: J1.048.665C
• Wikidata: Q82256655
• Mol file: 220967-27-1.mol

Synonyms:220967-27-1;5-amino-6-(4-methoxyphenyl)pyridazin-3(2H)-one;CTK0J6715;4-Amino-3-(4-methoxyphenyl)-1H-pyridazin-6-one;DTXSID60440367;6-(4-Methoxyphenyl)-5-aminopyridazine-3(2H)-one

Chemical Property of 5-amino-6-(4-methoxyphenyl)pyridazin-3(2H)-one

Chemical Property:

• Melting Point: 265 °C(Solv: N,N-dimethylformamide (68-12-2))
• PSA: 81.26000
• Density: 1.34±0.1 g/cm3(Predicted)
• LogP: 2.02120
• XLogP3: 0.8
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• Exact Mass: 217.085126602
• Heavy Atom Count: 16
• Complexity: 341

Purity/Quality:

5-amino-6-(4-methoxyphenyl)-3(2H)-Pyridazinone 97.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC1=CC=C(C=C1)C2=NNC(=O)C=C2N

Technology Process of 5-amino-6-(4-methoxyphenyl)pyridazin-3(2H)-one

There total 4 articles about 5-amino-6-(4-methoxyphenyl)pyridazin-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: 50.0%

5-bromo-6-(4'-methoxyphenyl)-3(2H)-pyridazinone (15904-55-9) → 5-amino-6-(4'-methoxyphenyl)-3(2H)-pyridazinone (220967-27-1)

Guidance literature:

With ammonium hydroxide; ammonium chloride; at 184 ℃; for 2.5h; under 19341.3 Torr;

DOI:10.1002/jhet.5570350634

Reference yield:

4-(4'-methoxyphenyl)-2,3-dibromocrotonolactone (4499-39-2) → 5-amino-6-(4'-methoxyphenyl)-3(2H)-pyridazinone (220967-27-1)

Guidance literature:

Multi-step reaction with 3 steps

1: 76 percent / MgO, H₂O / dioxane / 1.25 h / Heating

2: hydrazine hydrate / ethane-1,2-diol

3: 50 percent / ammonium chloride, ammonium hydroxide / 2.5 h / 184 °C / 19341.3 Torr

With ammonium hydroxide; ammonium chloride; water; magnesium oxide; hydrazine hydrate; In 1,4-dioxane; ethylene glycol;

DOI:10.1002/jhet.5570350634

Reference yield:

(E)-3-bromo-3-(4'-methoxybenzoyl)acrylic acid (16170-76-6,21653-96-3,5711-40-0) → 5-amino-6-(4'-methoxyphenyl)-3(2H)-pyridazinone (220967-27-1)

Guidance literature:

Multi-step reaction with 2 steps

1: hydrazine hydrate / ethane-1,2-diol

2: 50 percent / ammonium chloride, ammonium hydroxide / 2.5 h / 184 °C / 19341.3 Torr

With ammonium hydroxide; ammonium chloride; hydrazine hydrate; In ethylene glycol;

DOI:10.1002/jhet.5570350634

upstream raw materials:

5-bromo-6-(4'-methoxyphenyl)-3(2H)-pyridazinone

4-(4'-methoxyphenyl)-2,3-dibromocrotonolactone

(E)-3-bromo-3-(4'-methoxybenzoyl)acrylic acid

methoxybenzene

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