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5-Chloropyrazolo[1,5-a]pyrimidine

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5-Chloropyrazolo[1,5-a]pyrimidine Basic information

Product Name:
5-Chloropyrazolo[1,5-a]pyrimidine
Synonyms:
  • 5-CHLOROPYRAZOLO[1,5-A]PYRIMIDINE
  • 5-Chloropyrazolo[1,5-a]py...
  • 5-Chloropyrazolo[1,5-a]pyrimidine 97%
  • Larotrectinib Impurity 2(Larotrectinib CPP Impurity)
  • Pyrazolo[1,5-a]pyriMidine, 5-chloro-
  • 5-chloro-4,5-dihydropyrazolo[1,5-a]pyrimidine
  • WEPRLWNMBTYGGD-UHFFFAOYSA-N
  • Larotrectinib CPP Impurity
CAS:
29274-24-6
MF:
C6H4ClN3
MW:
153.57
EINECS:
000-000-0
Product Categories:
  • Heterocycle-Pyrimidine series
  • 29274-24-6
Mol File:
29274-24-6.mol
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5-Chloropyrazolo[1,5-a]pyrimidine Chemical Properties

Density 
1.51±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
-0.49±0.30(Predicted)
Appearance
Light brown to yellow Solid
InChI
InChI=1S/C6H4ClN3/c7-5-2-4-10-6(9-5)1-3-8-10/h1-4H
InChIKey
WEPRLWNMBTYGGD-UHFFFAOYSA-N
SMILES
C12=CC=NN1C=CC(Cl)=N2
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Safety Information

RIDADR 
UN2811
HazardClass 
IRRITANT
HS Code 
2933599590
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5-Chloropyrazolo[1,5-a]pyrimidine Usage And Synthesis

Uses

5-Chloropyrazolo[1,5-a]pyrimidine was used in the preparation of β-substituted biarylphenylalanine amides as selective amino amide dipeptidyl peptidase IV inhibitors for treatment of type 2 diabetes.

Synthesis

29274-22-4

29274-24-6

General procedure for the synthesis of 5-chloropyrazolo[1,5-a]pyrimidin-5-ol from pyrazolo[1,5-a]pyrimidin-5-ol: Pyrazolo[1,5-a]pyrimidin-5-ol (17.0 g, 126 mmol) was dissolved in phosphorus triclosan (100 mL) and heated to reflux for 3 hours. Upon completion of the reaction, the reaction was cooled to room temperature and the reaction mixture was concentrated under reduced pressure to remove excess phosphorous trichloride. Dichloromethane (100 mL) was added to the residue to dissolve it, followed by careful washing of the organic phase with saturated aqueous sodium bicarbonate solution (100 mL x 3) to neutralize acidic impurities. The organic phase was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give the crude product. The crude product was purified by short silica gel column chromatography, using 50% ethyl acetate in hexane solution as eluent, the target fraction was collected and concentrated under reduced pressure to give 5-chloropyrazolo[1,5-a]pyrimidine (13.1 g, 68% yield).

References

[1] Patent: WO2011/29027, 2011, A1. Location in patent: Page/Page column 42
[2] Patent: US2016/168156, 2016, A1. Location in patent: Paragraph 0350; 0354; 0355
[3] Patent: WO2013/12915, 2013, A1. Location in patent: Paragraph 00681
[4] Patent: WO2014/151147, 2014, A1. Location in patent: Paragraph 00641
[5] Patent: US9295673, 2016, B2. Location in patent: Page/Page column 351

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