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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40928Generated: October 26, 2026

4-Bromo-1H-pyrrolo[2,3-b]pyridine → 3-[1-(1H-Pyrrolo[2,3-b]pyridin-4-yl)-1H-pyrazol-4-yl]benzonitrile

https://huagongshe.com/reaction/40928

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-1H-pyrrolo[2,3-b]pyridineHCID 22273643—
Reactant3-(1H-pyrazol-4-yl)benzonitrile trifluoroacetateHCID 66597404—
Product3-[1-(1H-Pyrrolo[2,3-b]pyridin-4-yl)-1H-pyrazol-4-yl]benzonitrileHCID 57477665—

Reaction Conditions

Temperature180 °C

Reaction Steps

A mixture of 4-bromo-1H-pyrrolo[2,3-b]pyridine (25.0 mg, 0.000127 mol) and 3-(1H-pyrazol-4-yl)benzonitrile trifluoroacetate (23.6 mg, 0.0000833 mol) was heated at 180° C., neat overnight. The crude residue was purified by HPLC on a C-18 column eluting with a water; ACN gradient containing 0.2% TFA to give the title compound as an amorphous white solid, LC/MS (M+H)+: 286, 1H NMR (DMSO-d6) δ 11.85 (bs, 1H), 9.18(s, 1H), 8.42(s, 1H), 8.28(s, 1H), 8.25(d, 1H, J=5.0), 8.07(d, 1H, J=7.0), 7.64(d, 1H, J=7.0), 7.56(t, 1H, J=7.0), 7.51(m, 1H), 7.47(d, 1H, J=5.0), 7.03(m,1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530485B2
Source datasetuspto-grants-2013_09
ORD IDord-13de056aa4af4d6ba0b43915f327c812
Source noteuspto-grants-2013_09