5-Amino-1-ethyl-3-methyl-1H-pyrazole-4-carbonitrile

Base Information

• Chemical Name: 5-Amino-1-ethyl-3-methyl-1H-pyrazole-4-carbonitrile
• CAS No.: 102997-29-5
• Molecular Formula: C7H10N4
• Molecular Weight: 150.18100
• Hs Code.: 2933199090
• DSSTox Substance ID: DTXSID60444603
• Wikidata: Q82262791
• Mol file: 102997-29-5.mol

Synonyms:102997-29-5;5-AMINO-1-ETHYL-3-METHYL-1H-PYRAZOLE-4-CARBONITRILE;5-AMINO-1-ETHYL-3-METHYLPYRAZOLE-4-CARBONITRILE;5-amino-1-ethyl-3-methyl-pyrazole-4-carbonitrile;SCHEMBL7302490;DTXSID60444603;CEA99729;AKOS006295707;EN300-1617911

Chemical Property of 5-Amino-1-ethyl-3-methyl-1H-pyrazole-4-carbonitrile

Chemical Property:

• PSA: 67.63000
• LogP: 1.24648
• Storage Temp.: 2-8°C
• XLogP3: 0.9
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 150.090546336
• Heavy Atom Count: 11
• Complexity: 182

Purity/Quality:

99% ，98% ^*data from raw suppliers

5-Amino-1-ethyl-3-methyl-1H-pyrazole-4-carbonitrile 95+% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCN1C(=C(C(=N1)C)C#N)N

Technology Process of 5-Amino-1-ethyl-3-methyl-1H-pyrazole-4-carbonitrile

There total 3 articles about 5-Amino-1-ethyl-3-methyl-1H-pyrazole-4-carbonitrile 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: 76.7%

5-amino-4-cyano-3-methyl-1-vinyl-(1H)-pyrazole → 5-amino-4-cyano-3-methyl-1-ethyl-(1H)-pyrazole (102997-29-5)

Guidance literature:

palladium; In ethyl acetate;

Reference yield: 73.0%

ethylhydrazine (624-80-6) + 2-cyano-3-ethoxythiocrotonamide (89943-20-4) → 5-amino-4-cyano-3-methyl-1-ethyl-(1H)-pyrazole (102997-29-5) + 1-ethyl-3-methyl-4-thiocarbamoyl-5-aminopyrazole (101309-70-0)

Guidance literature:

In water; Ambient temperature;

DOI:10.1002/jhet.5570220434

Reference yield:

ethylhydrazine oxalic acid salt (6629-60-3) + (1-ethoxyethylidene)malononitrile (5417-82-3) → 5-amino-4-cyano-3-methyl-1-ethyl-(1H)-pyrazole (102997-29-5)

Guidance literature:

With sodium methylate; Yield given. Multistep reaction; 1.) CH₃OH, reflux, 15 min, 2.) CH₃OH, reflux, 2 h;

DOI:10.1021/jm950812j

upstream raw materials:

ethylhydrazine

2-cyano-3-ethoxythiocrotonamide

ethylhydrazine oxalic acid salt

(1-ethoxyethylidene)malononitrile

Downstream raw materials:

N-(4-Cyano-2-ethyl-5-methyl-2H-pyrazol-3-yl)-5-nitro-2-propoxy-benzamide

1-Ethyl-3-methyl-6-(2-propoxy-phenyl)-1,5-dihydro-pyrazolo[3,4-d]pyrimidin-4-one

1-ethyl-3-methyl-6-(5-bromo-2-propoxyphenyl)-1,5-dihydro-pyrazolo[3,4-d]pyrimidin-4-one

1-Ethyl-3-methyl-6-(2-propoxy-5-aminophenyl)-1,5-dihydro-pyrazolo[3,4-d]pyrimidin-4-one