HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-Aminoquinoline → 9H-Fluorene-2-carboxylic acid quinolin-7-yl amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-Aminoquinoline | HCID 11377 | — |
| Reactant | 9H-fluorene-2-carboxylic acid | HCID 348591 | — |
| Product | 9H-Fluorene-2-carboxylic acid quinolin-7-yl amide | HCID 57682733 | — |
Reaction Steps
Using the procedure outlined in Example 56, the title compound was prepared from 7-aminoquinoline (D55) (50 mg, 0.35 mmol) and 9H -fluorene-2-carboxylic acid (D71) (83 mg, 0.38 mmol) as an off-white solid. MS(ES): MH+ 337, M-H+ 335.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07538121B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-55f03debc4054ef3b9542e462682614a |
| Source note | uspto-grants-2009_05 |