3-Bromo-1-(3-Chloro-2-Pyridinyl)-1H-Pyrazole-5-Carboxylic Acid(K Acid)

CAS No: 500011-86-9
Chemical Name: 3-BroMo-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxylic acid
Synonyms: 3-broMo-1-(3-chloro-2-pyridinyl)-1H-Pyrazole-5-carboxylic acid; 3-Bromo-1-(3-chloropyridin-2-yl); 5-Bromo-2-(3-chloro-2-pyridyl)pyrazole-3-carboxylic acid; 5-Bromo-2-(3-chloro-pyridin-2-yl)-2H-pyrazole-3-carboxylic acid; cas 500011-86-9; cas 500011-86-9 95%; coragen intermediate; Chlorantranliprole intermediate; intermediate of Chlorantranliprole; cas 500011-86-9 Coragen intermediate
CBNumber: CB12550168
Molecular Formula: C₉H₅BrClN₃O₂
Molecular Weight: 302.51
MDL Number: MFCD08689880
SKU: K Acid Categories: ,

A Acid Properties

  Melting point   197-200 °C
  Boiling point   477.4±45.0 °C(Predicted)
  Density   1.92±0.1 g/cm3(Predicted)
  vapor pressure   0Pa at 20℃
  storage temp.   2-8°C
  solubility   DMSO (Slightly), Methanol (Slightly)
  form   Solid
  pka   2.39±0.36(Predicted)
  color   White to Light Brown
  Water Solubility   8.84g/L at 20.3℃
  InChI   InChI=1S/C9H5BrClN3O2/c10-7-4-6(9(15)16)14(13-7)8-5(11)2-1-3-12-8/h1-4H,(H,15,16)
  InChIKey   FORBXGROTPOMEH-UHFFFAOYSA-N
  SMILES   N1(C2=NC=CC=C2Cl)C(C(O)=O)=CC(Br)=N1
  LogP   1.5 at 25℃

Uses

3-Bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxylic acid is a useful building block and has been used in the synthesis of the pesticide Cyclaniliprole.

Synthesis

Pyridine, 2-(3-broMo-1H-pyrazol-1-yl)-3-chloro-     +      Carbon dioxide      →        3-BroMo-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxylic acid

At -78 °C, 2-(3-bromo-1H-pyrazol-1-yl)-3-chloropyridine (3.04 g, 11.8 mmol) was dissolved in anhydrous THF (25 mL), keeping the reaction temperature below -71 °C. LDA solution (6 mL, 2M) was added slowly and dropwise. The reaction mixture was stirred at -78 °C for 15 min and then bubbled with carbon dioxide gas for 10 min. Subsequently, the reaction system was slowly warmed to -57°C and continued to -20°C. Upon completion of the reaction, the reaction was quenched with water. The reaction mixture was concentrated and dissolved in water (100 mL) and ether (80 mL), and an aqueous NaOH solution (1N, 2 mL) was added. The aqueous phase was washed with ether and acidified with aqueous HCl (2N). The precipitated solid was filtered, washed with water and dried to give 3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxylic acid (2 g, 59% yield) as a brown solid.

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