Basic information Safety Supplier Related

1H-Pyrazole-5-carboxaMide, 1-Methyl-4-[(2-propoxybenzoyl)aMino]-3-propyl-

Basic information Safety Supplier Related

1H-Pyrazole-5-carboxaMide, 1-Methyl-4-[(2-propoxybenzoyl)aMino]-3-propyl- Basic information

Product Name:
1H-Pyrazole-5-carboxaMide, 1-Methyl-4-[(2-propoxybenzoyl)aMino]-3-propyl-
Synonyms:
  • 1H-Pyrazole-5-carboxaMide, 1-Methyl-4-[(2-propoxybenzoyl)aMino]-3-propyl-
  • 3-[[[5-(AMinocarbonyl)-1-Methyl-3-propyl-1H-pyrazol-4-yl]aMino]carbonyl]-4-propoxybenzene
  • 2-methyl-4-[(2-propoxybenzoyl)amino]-5-propylpyrazole-3-carboxamide
  • 1-Methyl-4-(2-propoxybenzamido)-3-propyl-1H-pyrazole-5-carboxamide
  • 1-Methyl-4-(2-n-propoxybenzamido)-3-n-propylpyrazole-5-carboxamide
  • 2-Methyl-4-(2-propoxy-benzoylamino)-5-propyl-2h-pyrazole-3-carboxylic acid amide
  • 4-(2-Propoxybenzoylamino)-1-methyl-3-propyl-1H-pyrazole-5-carboxamide
  • Sildenafil Impurity 56
CAS:
139756-04-0
MF:
C18H24N4O3
MW:
344.41
Product Categories:
  • Aromatics
  • Heterocycles
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • Aromatics, Heterocycles, Pharmaceuticals, Intermediates & Fine Chemicals
Mol File:
139756-04-0.mol
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1H-Pyrazole-5-carboxaMide, 1-Methyl-4-[(2-propoxybenzoyl)aMino]-3-propyl- Chemical Properties

Melting point:
>140°C
storage temp. 
2-8°C
solubility 
Chloroform (Slightly), Methanol (Slightly)
form 
Solid
color 
White to Off-White
InChI
InChI=1S/C18H24N4O3/c1-4-8-13-15(16(17(19)23)22(3)21-13)20-18(24)12-9-6-7-10-14(12)25-11-5-2/h6-7,9-10H,4-5,8,11H2,1-3H3,(H2,19,23)(H,20,24)
InChIKey
OYHROMDBMGIQCJ-UHFFFAOYSA-N
SMILES
N1(C)C(C(N)=O)=C(NC(=O)C2=CC=CC=C2OCCC)C(CCC)=N1
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1H-Pyrazole-5-carboxaMide, 1-Methyl-4-[(2-propoxybenzoyl)aMino]-3-propyl- Usage And Synthesis

Chemical Properties

Off-white Solid

Uses

Intermediate in the preparation of Sildenafil (S435000) analogues.

Synthesis

2100-31-4

139756-02-8

139756-04-0

Step 8 Synthesis of 2-methyl-4-(2-propoxybenzoylamino)-5-propyl-2H-pyrazole-3-carboxamide: 2-Propoxybenzoic acid (13.7 g, 76.1 mmol) was mixed with thionyl chloride (36.2 g, 304.4 mmol) in anhydrous dichloromethane (80 mL) and heated at reflux for 3 hours. Upon completion of the reaction, the solvent and excess thionyl chloride were removed by distillation under reduced pressure. The resulting chloride intermediate was dissolved in anhydrous dichloromethane (60 mL) and slowly added to an anhydrous solution containing 4-amino-2-methyl-5-propyl-2H-pyrazole-3-carboxamide (12.6 g, 69.2 mmol), dry triethylamine (7 g, 69.2 mmol), and 4-(N,N-dimethylamino)pyridine (84.5 mg, 0.7 mmol). dichloromethane (200 mL) solution, maintaining the reaction temperature at 0°C. After stirring the reaction mixture for 1 h, it was washed sequentially with water (150 mL), saturated aqueous sodium carbonate solution (200 mL) and saturated brine (200 mL). The organic layer was dried over anhydrous magnesium sulfate and filtered, the filtrate was concentrated to about 60 mL and a white solid product (22 g, 92% yield) was precipitated by addition of hexane (150 mL). The product was confirmed by 1H NMR (300 MHz, CDCl3) and LC-MS (m/z = 345 [M + H]+) characterization.

References

[1] Patent: US2008/194529, 2008, A1. Location in patent: Page/Page column 57-58
[2] Patent: US2003/176696, 2003, A1

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