HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494233Generated: October 29, 2026
7-Aminoquinoline → HCID 44415654, compound
https://huagongshe.com/reaction/494233
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 7-Aminoquinoline | HCID 11377 | — |
| Reactant | (1,1'-Biphenyl)-4-carboxylic acid | HCID 66724 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 44415654 | HCID 44415654 | — |
Reaction Steps
To a solution of 7-aminoquinoline (D55) (100 mg, 0.69 mmol) in DCM (3 ml) was added 4-biphenylcarboxylic acid (206 mg, 1.04 mmol), 1-(3-dimethylamino-propyl)-3-ethyl-carbodiimide hydrochloride (197 mg, 1.04 mmol) and 4-dimethylaminopyridine (10 mg, 0.08 mmol) and the reaction stirred at room temperature overnight. The mixture was diluted with DCM, washed with sat. aqueous sodium bicarbonate solution, dried over MgSO4 and concentrated in vacuo to give the crude product which was purified by SPE column chromatography. Elution with 50% EtOAc in 40-60° C. petroleum ether gave the title compound as an off-white solid. 1H NMR (400 MHz, CDCl3) δ (ppm): 8.91 (dd, 1H), 8.19 (d, 1H), 8.12 (m, 2H), 8.02, (d, 2H), 7.86 (d, 1H), 7.75 (d, 2H), 7.65 (d, 2H), 7.49 (t, 2H), 7.42 (t, 1H), 7.36 (dd, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07538121B2 |
|---|
| Source dataset | uspto-grants-2009_05 |
|---|
| ORD ID | ord-f0743b5440eb42188c0abcb4d36540f3 |
|---|
| Source note | uspto-grants-2009_05 |
|---|