HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 49868763, compound → HCID 49870791, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 49868763 | HCID 49868763 | — |
| Reactant | HCID 66831363 | HCID 66831363 | — |
| Product | HCID 49870791 | HCID 49870791 | — |
Reaction Steps
4-amino-6-(((1S)-1-(3-(3,5-difluorophenyl)-6-fluoro-4-oxo-1,4-dihydro-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile was synthesized from (S)-2-(1-(3-(3,5-difluorophenyl)-6-fluoro-4-oxo-1,4-dihydroquinolin-2-yl)ethyl)-isoindoline-1,3-dione in a similar manner as the above compound 4-amino-6-(1-(3-(3,5-difluorophenyl)-6-fluoro-1-methyl-4-oxo-1,4-dihydroquinolin-2-yl)-ethylamino)pyrimidine-5-carbonitrile. 1H-NMR (400 Hz, DMSO-d6) δ 11.50 (s, 1H), 7.97 (s, 1H), 7.69-7.73 (m, 2H), 7.59 (td, J=8.0, 4.0 Hz, 1H), 7.46 (s, br, 1H), 7.17-7.22 (m, 2H), 7.05 (s, br, 1H), 5.01-5.06 (m, 1H), 1.48 (t, J=8.0 Hz, 3H). Mass Spectrum (ESI) m/e=437 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08754089B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-bb826bd2d3f74e74a721d8d091dfa128 |
| Source note | uspto-grants-2014_06 |