HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-methylquinoline-4-carboxylic Acid → HCID 86714313, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-methylquinoline-4-carboxylic Acid | HCID 6460899 | — |
| Reactant | (R)-2-(((4-amino-2,2-dioxido-1H-benzo[c][1,2,6]thiadiazin-5-yl)oxy)methyl)piperidinium hydrochloride | HCID 86714283 | — |
| Product | HCID 86714313 | HCID 86714313 | — |
Reaction Steps
Prepared as in Example 15 from (R)-2-(((4-amino-2,2-dioxido-1H-benzo[c][1,2,6]thiadiazin-5-yl)oxy)methyl)piperidinium hydrochloride (Example 15a) and 6-methylquinoline-4-carboxylic acid. 1H NMR (400 MHz, DMSO-d6) δ 1.34-1.53 (m, 2H), 1.59-1.86 (m, 4H), 2.01 (s, 3H), 3.01 (m, 1H), 3.20 (m, 1H), 4.19 (dd, 1H, J=10.1, 3.2 Hz), 4.95 (t, 1H, J=10.6 Hz), 5.46 (m, 1H), 6.67 (d, 1H, J=8.1 Hz), 7.01 (d, 1H, J=8.3 Hz,), 7.34 (s, 1H), 7.48-7.56 (m, 2H), 7.60-7.68 (m, 1H), 7.92 (d, 1H, J=8.7 Hz), 7.99 (br s, 1H), 8.27 (br s, 1H), 8.87 (d, 1H, J=4.4 Hz), 10.94 (s, 1H). MS 480 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09138013B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-e2c67e3f225741ca9530ba5b84dc0ccf |
| Source note | uspto-grants-2015_09 |