HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylamine → 6-Chloro-2-(3-dimethylamino-cyclopentyl)-quinoline-5-carboxylic acid (1-hydroxy-3-methyl-cyclohexyl methyl)-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | 6-Chloro-2-(3-oxo-cyclopentyl)-quinoline-5-carboxylic acid (1-hydroxy-3-methyl-cyclohexylmethyl)-amide | HCID 131736447 | — |
| Product | 6-Chloro-2-(3-dimethylamino-cyclopentyl)-quinoline-5-carboxylic acid (1-hydroxy-3-methyl-cyclohexyl methyl)-amide | HCID 118566688 | — |
Reaction Steps
The title compound was synthesized according to the procedure described in example 133 using 6-chloro-2-(3-oxo-cyclopentyl)-quinoline-5-carboxylic acid (1-hydroxy-3-methylcyclohexyl methyl)-amide, and dimethylamine. 1H NMR (400 MHz, DMSO-d6) δ ppm (VTNMR: 80° C.): 8.26-8.24 (m, 1H), 8.11-8.09 (m, 1H), 7.97-7.94 (m, 1H), 7.73-7.70 (m, 1H), 7.56-7.54 (m, 1H), 3.87-3.85 (m, 1H), 3.46-3.33 (m, 3H), 2.77-2.49 (m, 1H), 2.25-1.34 (m, 20H), 0.87-0.77 (m, 1H). m/z: 444.0 [M+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09399623B2 |
| Source dataset | uspto-grants-2016_07 |
| ORD ID | ord-f397f249934e4003be1690018a82a01a |
| Source note | uspto-grants-2016_07 |