Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615345Generated: October 30, 2026

2-Oxo-2,3-dihydro-1H-indole-5-carbonitrile → HCID 178509446, compound

https://huagongshe.com/reaction/1615345

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Oxo-2,3-dihydro-1H-indole-5-carbonitrileHCID 2773346—
ReactantHCID 86651957HCID 86651957—
ProductHCID 178509446HCID 178509446—

Reaction Steps

The title compound was synthesized according to the method described in Example A57 from 2-oxoindoline-5-carbonitrile (10 mg, 0.063 mmol) and (E)-3-(2-(pyridin-4-yl)vinyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-indazole-6-carbaldehyde (25 mg, 0.063 mmol) with a modified purification procedure. The product was precipitated with EtOAc and filtered washing with EtOAc to give 4.5 mg, 30% of a yellow powder which was a 65:35 mixture of (E)/(Z) isomers. 1H NMR (400 MHz, d6-DMSO) δ 14.04, 13.94 (s, 1H), 11.24, 11.22 (s, 1H), 9.01, 8.42 (s, 1H), 8.83 (d, J=5.5 Hz, 2H), 8.50-8.17 (m, 3H), 8.03 (s, 1H), 7.99 (s, 1H), 7.86 (s, 1H), 7.81-7.65 (m, 3H), 7.07, 7.01 (d, J=8.4 Hz, 1H); MS ESI 390.1 [M+H]+, calcd for [C24H15N5O+H]+ 390.14.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765748B2
Source datasetuspto-grants-2014_07
ORD IDord-b00b7be20d624c64a56cf27caf534aab
Source noteuspto-grants-2014_07