HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-Aminoquinoline → 2-Methyl-N-quinolin-7-yl-1,1'biphenyl-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-Aminoquinoline | HCID 11377 | — |
| Reactant | 2-Methyl-[1,1'-biphenyl]-4-carboxylic acid | HCID 21521810 | — |
| Product | 2-Methyl-N-quinolin-7-yl-1,1'biphenyl-4-carboxamide | HCID 57682726 | — |
Reaction Steps
Using the procedure outlined in Example 56, the title compound was prepared from 7-aminoquinoline (D55) (30 mg, 0.21 mmol) and 2-methyl-1,1′-biphenyl-4-carboxylic acid (D60) (53 mg, 0.25 mmol) as a white solid. MS(ES): MH+ 339
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07538121B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-04ea3e4682b14397b1955f56b16ae808 |
| Source note | uspto-grants-2009_05 |