HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Methylnicotinic acid → HCID 59631432, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Methylnicotinic acid | HCID 137860 | — |
| Reactant | 5,7-difluoro-3-methyl-N-(5-morpholinopyridin-3-yl)-2-(piperazin-1-yl)quinolin-4-amine | HCID 59631028 | — |
| Product | HCID 59631432 | HCID 59631432 | — |
Reaction Steps
Prepared according to Procedure Q using 5,7-difluoro-3-methyl-N-(5-morpholinopyridin-3-yl)-2-(piperazin-1-yl)quinolin-4-amine (40.0 mg, 0.09 mmol) and 6-methylnicotinic acid to give (4-(5,7-difluoro-3-methyl-4-(5-morpholinopyridin-3-ylamino)quinolin-2-yl)piperazin-1-yl)(6-methylpyridin-3-yl)methanone. 1H NMR (DMSO-d6) δ ppm 2.09 (br s, 3H), 2.50-2.52 (m, 4H), 3.03-3.05 (m, 4H), 3.33-3.40 (m, 3H), 3.55 (br s, 2H), 3.67-3.69 (m, 4H), 3.82 (br s, 2H), 6.49 (s, 1H), 7.14-7.20 (m, 1H), 7.30-7.26 (m, 1H), 7.35-7.37 (m, 1H), 7.51 (d, J=2.4 Hz, 1H), 7.78 (br s, 2H), 8.37 (s, 1H), 8.54 (d, J=2.4 Hz, 1H). Mass Spectrum (ESI) m/e=560.4 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08940724B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-8f3e700005f0445fb95303c857c20654 |
| Source note | uspto-grants-2015_01 |