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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615288Generated: November 1, 2026

1,3-Dihydro-2H-pyrrolo(2,3-b)pyridin-2-one → HCID 178517367, compound

https://huagongshe.com/reaction/1615288

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dihydro-2H-pyrrolo(2,3-b)pyridin-2-oneHCID 13864095—
ReactantHCID 86651961HCID 86651961—
ProductHCID 178517367HCID 17851736728.2%

Reaction Steps

The title compound (7 mg, 21%) was synthesized as yellow solid according to the method described for Example A67 using 1H-pyrrolo[2,3-b]pyridin-2(3H)-one (9.3 mg, 0.07 mmol) and (E)-3-(2-(pyridin-2-yl)vinyl)-1H-indazole-6-carbaldehyde (17 mg, 0.068 mmol). 1H NMR (400 MHz, DMSO-d6) δ 13.53 (s, 1H, NH), 11.27 (s, 1H, NH), 8.62 (d, J=4.0 Hz, 1H), 8.35 (d, J=8.4 Hz, 1H), 8.12 (d, J=5.2 Hz, 1H), 8.02-7.89 (m, 4H), 7.82 (t, J=8.0 Hz, 1H), 7.69 (d, J=7.6 Hz, 1H), 7.63 (d, J=16.8 Hz, 1H), 7.56 (d, J=8.4 Hz, 1H), 7.28 (t, J=6.0 Hz, 1H), 6.91 (dd, J=7.6 Hz, 5.6 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-5630e292273c47a0bf7c246e18608d71
Source noteuspto-grants-2014_07