HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-Aminoquinoline → 4-(2-Methylthiazol-4yl)-N-quinolin-7-yl-benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-Aminoquinoline | HCID 11377 | — |
| Reactant | 4-(2-Methyl-1,3-thiazol-4-yl)benzoic acid | HCID 654980 | — |
| Product | 4-(2-Methylthiazol-4yl)-N-quinolin-7-yl-benzamide | HCID 57682665 | — |
Reaction Steps
Using the procedure outlined in Example 56, the title compound was prepared from 7-aminoquinoline (D55) (27 mg, 0.19 mmol) and 4-(2-methylthiazol-4-yl)-benzoic acid (D87) (50 mg, 0.23 mmol) as a solid. MS(ES): MH+ 346, M-H+ 344
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07538121B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-b91ac506029846fd96a4211541561e39 |
| Source note | uspto-grants-2009_05 |