HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 11462285, compound → HCID 59655980, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 11462285 | HCID 11462285 | — |
| Reactant | HCID 86595727 | HCID 86595727 | — |
| Product | HCID 59655980 | HCID 59655980 | — |
Reaction Steps
Arylation of 4-(5-chloro-1H-indol-3-yl)-4-oxo-butyric acid 2-trimethylsilanyl-ethyl ester with 1-(4-chloro-6-phenyl-[1,3,5]-triazin-2-yl)-1,2,3,4-tetrahydro-quinoline and subsequent hydrolysis as outlined previously yielded the titled compound. Rf 0.34 (5% methanol in dichloromethane); 1H NMR (THF-d8, 300 MHz) δ 9.21 (1H, s, ArH), 8.72 (1H, m, ArH), 8.59 (2H, d, J=7 Hz, ArH), 8.39 (1H, d, J=2 Hz, ArH), 7.95 (1H, d, J=8 Hz, ArH), 7.62-7.51 (3H, m, ArH), 7.35-7.15 (4H, m, ArH), 4.32 (2H, t, J=6 Hz, CH2), 3.30 (2H, t, J=7 Hz, CH2), 2.88 (2H, t, J=6 Hz, CH2), 2.72 (2H, t, J=7 Hz, CH2), 2.13 (2H, m, CH2); ESI-LCMS e/z calculated for C30H24ClN5O3 537.157, found 538 (M+H)+, 560 (M+Na)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07329680B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-71db438701764606af5c8ceff8abecef |
| Source note | uspto-grants-2008_02 |