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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615310Generated: October 31, 2026

1,3-Dihydro-2H-pyrrolo(2,3-b)pyridin-2-one → HCID 178517369, compound

https://huagongshe.com/reaction/1615310

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dihydro-2H-pyrrolo(2,3-b)pyridin-2-oneHCID 13864095—
ReactantHCID 86651972HCID 86651972—
ProductHCID 178517369HCID 17851736987.6%

Reaction Steps

The title compound (64 mg, 64%) was synthesized as orange red solid according to the method described for Example A11B from 1H-pyrrolo[2,3-b]pyridin-2(3H)-one (26.8 mg, 0.2 mmol) and E)-3-(2-(pyridin-4-yl)vinyl)-1H-indazole-6-carbaldehyde (49.8 mg, 0.2 mmol). 1H NMR (400 MHz, DMSO-d6) δ 13.60 (s, 1H, NH), 11.28 (s, 1H, NH), 8.57 (d, J=5.6 Hz, 2H), 8.39 (d, J=8.4 Hz, 1H), 8.12 (d, J=4.8 Hz, 1H), 7.95 (s, 2H), 7.90 (d, J=6.4 Hz, 1H, partially overlapping with the peak at 7.87 ppm), 7.87 (d, J=16.4 Hz, 1H, partially overlapping with the peak at 7.90 ppm), 7.71 (d, J=5.6 Hz, 2H), 7.57 (d, J=8.0 Hz, 1H, partially overlapping with the peak at 7.56 ppm), 7.56 (d, J=16.4 Hz, 1H, partially overlapping with the peak at 7.57 ppm), 6.91 (dd, J=7.6 Hz, 5.2 Hz, 1H); MS ESI 366.1 [M+H]+, calcd for [C22H15N5O+H]+ 366.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765748B2
Source datasetuspto-grants-2014_07
ORD IDord-549fe36cab774c8c92f8511591f00de9
Source noteuspto-grants-2014_07