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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2375941Generated: October 31, 2026

Trifluoroacetic acid → HCID 59854563, compound

https://huagongshe.com/reaction/2375941

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant1H-IndazoleHCID 9221—
ReactantHCID 59854535HCID 59854535—
ReactantHCID 59854553HCID 59854553—
SolventMethanolHCID 887—
Solvent2,2,2-TrifluoroethanolHCID 6409—
SolventSodium BicarbonateHCID 516892—
ProductHCID 59854563HCID 59854563—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a slurry of a mixture of 1-benzenesulfonyl-5-bromo-4-chloro-2-iodo-1H-pyrrolo[2,3-b]pyridine and 5-bromo-4-chloro-2-iodo-1-(2-iodobenzenesulfonyl)-1H-pyrrolo[2,3-b]pyridine (560 mg, 1.0 mmol) in trifluoroethanol (6 mL) was added trifluoroacetic acid (0.041 mL, 0.52 mmol) and indazole (266 mg, 2.0 mmol), and the reaction was heated in a sealed tube at 120° C. for 4 d. Additional indazole (67 mg, 0.5 mmol) was added twice to the reaction on the second and third days. The reaction was cooled to RT, diluted with methanol (20 mL), saturated sodium bicarbonate solution was added (1 mL) and evaporated to dryness under reduced pressure. The residue obtained was triturated with methanol:DCM (1:1) mixture and filtered. The filtrate was evaporated and the crude obtained was purified by chromatography on silica gel [Jones Flashmaster, 70 g/150 mL cartridge, eluting with DCM:Methanol 100:0→96:4], yielding the product, which was triturated with 4:1 methanol:DCM mixture and filtered. The precipitate obtained was dried under vacuum to afford the title compound as an off-white solid. The low polar fractions from the column were combined, evaporated and the residue was stirred with 3N NaOH in methanol (2 mL) for 30 min and quenched with saturated ammonium chloride solution (2 mL). Water (10 mL) was added and filtered to afford additional title compound. MS (ES+): m/z 453.63 (100) [MH+]; HPLC: tR=2.58 min (ZQ2000, polar—5 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07465726B2
Source datasetuspto-grants-2008_12
ORD IDord-82d642c769f84621adb54d0307621f3d
Source noteuspto-grants-2008_12