HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-Aminoquinoline → 3-Methoxy-N-quinolin-7-yl-1,1'biphenyl-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-Aminoquinoline | HCID 11377 | — |
| Reactant | 2-Methoxy-4-phenylbenzoic acid | HCID 18687407 | — |
| Product | 3-Methoxy-N-quinolin-7-yl-1,1'biphenyl-4-carboxamide | HCID 57682686 | — |
Reaction Steps
Using the procedure outlined in Example 56, the title compound was prepared from 7-aminoquinoline (D55) (26 mg, 0.18 mmol) and 3-methoxy-1,1′-biphenyl-4-carboxylic acid (D59) (50 mg, 0.22 mmol) as an off-white solid. MS (ES): MH+ 355.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07538121B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-ab9e945985684653980d7f86cce33d32 |
| Source note | uspto-grants-2009_05 |