HuagongsheHuagongshe Chemistry Print Report · For research reference only
202599-49-3 → HCID 69200844, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 202599-49-3 | HCID 230593 | — |
| Reactant | 5'-amino-N-(cyclopropylmethyl)-2'-methyl-1,1'-biphenyl-4-carboxamide | HCID 11300488 | — |
| Product | HCID 69200844 | HCID 69200844 | — |
Reaction Steps
N-(4′-{[(Cyclopropylmethyl)amino]carbonyl}-6-methyl-1,1′-biphenyl-3-yl)-2-piperidin-1-ylquinoline-4- carboxamide was prepared from 5′-amino-N-(cyclopropylmethyl)-2′-methyl-1, 1′-biphenyl-4-carboxamide and 2-(piperidin-1-yl)quinoline-4-carboxylic acid using method B. NMR; δH CDCl3 7.90,(1H, d), 7.83-7.78,(4H, m), 7.67,(1H, b), 7.52,(1H, t), 7.42,(2H, d), 7.33,(1H, d), 7.26, (1H, m), 7.21,(1H, t), 7.01,(1H, s), 6.30,(1H, t), 3.63,(4H, s), 3.31,(2H, m), 2.27,(3H, s), 1.62,(6H, m), 1.07,(1H, m), 0.57,(2H, m), 0.28,(2H, m). LCMS: retention time 3.32 min, MH+519.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07432289B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-abe3b9afa95e40b4842f4f6023bf9437 |
| Source note | uspto-grants-2008_10 |