HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Oxo-2,3-dihydro-1H-indole-5-carbonitrile → HCID 178509446, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Oxo-2,3-dihydro-1H-indole-5-carbonitrile | HCID 2773346 | — |
| Reactant | HCID 86651957 | HCID 86651957 | — |
| Product | HCID 178509446 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08765748B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-b00b7be20d624c64a56cf27caf534aab |
| Source note | uspto-grants-2014_07 |