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6-Bromo-4-hydroxy-pyrazolo[1,5-a]pyridine-3-carbonitrile

Basic information Safety Supplier Related

6-Bromo-4-hydroxy-pyrazolo[1,5-a]pyridine-3-carbonitrile Basic information

Product Name:
6-Bromo-4-hydroxy-pyrazolo[1,5-a]pyridine-3-carbonitrile
Synonyms:
  • 6-Bromo-4-hydroxy-pyrazolo[1,5-a]pyridine-3-carbonitrile
  • Pyrazolo[1,5-a]pyridine-3-carbonitrile, 6-bromo-4-hydroxy-
CAS:
2068065-16-5
MF:
C8H4BrN3O
MW:
238.04
Mol File:
2068065-16-5.mol
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6-Bromo-4-hydroxy-pyrazolo[1,5-a]pyridine-3-carbonitrile Chemical Properties

Density 
1.88±0.1 g/cm3(Predicted)
pka
6.41±0.30(Predicted)
InChI
InChI=1S/C8H4BrN3O/c9-6-1-7(13)8-5(2-10)3-11-12(8)4-6/h1,3-4,13H
InChIKey
IFUVDUFAFVWZOT-UHFFFAOYSA-N
SMILES
C12=C(C#N)C=NN1C=C(Br)C=C2O
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6-Bromo-4-hydroxy-pyrazolo[1,5-a]pyridine-3-carbonitrile Usage And Synthesis

Uses

6-Bromo-4-hydroxy-pyrazolo[1,5-a]pyridine-3-carbonitrile is a pharmaceutical intermediate used in the preparation of Selpercatinib, an FDA-approved drug for the treatment of RET-positive advanced non-small cell lung cancer (NSCLC), thyroid cancer and certain other cancers

Synthesis

At room temperature, add 6-bromo-4-methoxypyrazolo[1,5-a]pyridine-3-carbonitrile (50g, 198.36mmol) and water (16.5mL, 916mmol) in a 1L single-neck flask in sequence, Sodium hydroxide (16.03g, 396.8mmol), DMA (500mL), stirred at room temperature for 5min, then transferred to 0°C, slowly added dodecanethiol (97mL, 397mmol), after the addition, the reaction was moved to 45°C overnight. Pour the reaction solution into 3L ice water, slowly add saturated citric acid water to adjust the PH=5, stir for half an hour, and then stand still filter, wash the filter cake with water and petroleum ether several times, and dry at 60°C to obtain 44.1g of yellow solid 6-Bromo-4-hydroxy-pyrazolo[1,5-a]pyridine-3-carbonitrile (6-Bromo-4-hydroxypyrazolo[1,5-a]pyridine-3-carbonitrile).

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