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