HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-Aminoquinoline → 3-Methyl-N-quinolin-7-yl-1,1'biphenyl-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-Aminoquinoline | HCID 11377 | — |
| Reactant | 3-Methyl-[1,1'-biphenyl]-4-carboxylic acid | HCID 14090570 | — |
| Product | 3-Methyl-N-quinolin-7-yl-1,1'biphenyl-4-carboxamide | HCID 57682750 | — |
Reaction Steps
Using the procedure outlined in Example 56, the title compound was prepared from 7-aminoquinoline (D55) (31, 0.22 mmol) and 3-methyl-1,1′-biphenyl-4-carboxylic acid (D58) (55 mg, 0.26 mmol) as an off-white solid. 1H NMR (400 MHz, CDCl3) δ (ppm): 8.91(dd, 1H), 8.14 (m, 3H), 7.86 (d, 1H), 7.78 (br, 1H), 7.66 (d, 1H), 7.62 (d, 2H), 7.53 (m, 2H), 7.48 (t, 2H), 7.40 (t, 1H), 7.36 (dd, 1H), 2.63 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07538121B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-b12b87bceaaa43da960f1c4274306f1c |
| Source note | uspto-grants-2009_05 |