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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58106Generated: October 30, 2026

Sodium Bicarbonate → 6-methyl-5-(6-(trifluoromethyl)-1H-indazol-4-yl)picolinamide

https://huagongshe.com/reaction/58106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant6-methyl-5-(6-(trifluoromethyl)-1H-indazol-4-yl)picolinonitrileHCID 89782931—
SolventAcetic AcidHCID 176—
SolventSulfuric AcidHCID 1118—
Product6-methyl-5-(6-(trifluoromethyl)-1H-indazol-4-yl)picolinamideHCID 8978323734%

Reaction Steps

6-Methyl-5-(6-(trifluoromethyl)-1H-indazol-4-yl)picolinonitrile (0.02 g, 0.066 mmol) in acetic acid (2 mL) and H2SO4 (2 mL) was stirred at room temperature for 18 hours. The reaction mixture was subsequently poured into a conical flask containing ice and was carefully neutralized with NaHCO3 and extracted into DCM. The organic layer was dried over Na2SO4 and concentrated in vacuo. The residue was purified by preparative HPLC (Waters SunFire C18, 5 μm, 30 mm ID×75 mm column) eluting with a gradient of 45-55% ACN (containing 0.035% TFA) in water (containing 0.05% TFA) to give the title compound as white solid (0.32 g, 34%). 1H NMR (400 MHz, DMSO-d6) δ ppm 2.42 (s, 3H), 7.42 (d, J=1.26 Hz, 1H), 7.73 (br s, 1H), 7.90-8.08 (m, 3H), 8.14 (br s, 1H); ESI-MS m/z [M+H]+ calc'd for C15H11F3N4O, 321.1. found 321.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434743B2
Source datasetuspto-grants-2016_09
ORD IDord-a57eef7e65a748dda85c07464a2797f9
Source noteuspto-grants-2016_09