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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40722Generated: October 25, 2026

5-fluoro-2-[1-(4-methoxy-benzyl)-1H-pyrrolo[2,3-b]pyridin-5-yl]-oxazolo[5,4-b]pyridine → 5-fluoro-2-(1H-pyrrolo[2,3-b]pyridin-5-yl)-oxazolo[5,4-b]pyridine

https://huagongshe.com/reaction/40722

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-fluoro-2-[1-(4-methoxy-benzyl)-1H-pyrrolo[2,3-b]pyridin-5-yl]-oxazolo[5,4-b]pyridineHCID 58220157—
SolventTrifluoroacetic acidHCID 6422—
Product5-fluoro-2-(1H-pyrrolo[2,3-b]pyridin-5-yl)-oxazolo[5,4-b]pyridineHCID 445552836%

Reaction Conditions

Temperature170 °C

Reaction Steps

Crude 5-fluoro-2-[1-(4-methoxy-benzyl)-1H-pyrrolo[2,3-b]pyridin-5-yl]-oxazolo[5,4-b]pyridine from Step 2 was dissolved in TFA (0.5 mL) and heated by microwave to 170° C. for 25 min. The volatiles were then removed in vacuo and the resulting residue was purified by HPLC to afford 5-fluoro-2-(1H-pyrrolo[2,3-b]pyridin-5-yl)-oxazolo[5,4-b]pyridine (2.5 mg, 9.8 μmol, 6% yield). ES MS (M+H+)=255; 1H NMR δ (ppm) (DMSO-d6): 12.18 (1H, s), 9.04 (1H, d, J=2.10 Hz), 8.76 (1H, d, J=2.06 Hz), 8.44 (1H, dd, J=8.39, 7.10 Hz), 7.67 (1H, t, J=2.75 Hz), 7.31 (1H, d, J=8.40 Hz), 6.68 (1H, d, J=3.43 Hz); HRMS m/z 255.0675 (C13H7FN4O+H+ requires 255.0677).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530483B2
Source datasetuspto-grants-2013_09
ORD IDord-8d0bcf1766954255b647c761a9fbe553
Source noteuspto-grants-2013_09