HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494287Generated: October 26, 2026
(1,1'-Biphenyl)-4-carboxylic acid → N-(1-Methylisoquinolin-5-yl)-1,1'-biphenyl-4-carboxamide
https://huagongshe.com/reaction/494287
Participants
| Role | Name | HCID | Charge |
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| Reactant | (1,1'-Biphenyl)-4-carboxylic acid | HCID 66724 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 1-Methylisoquinolin-5-amine | HCID 9989490 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(1-Methylisoquinolin-5-yl)-1,1'-biphenyl-4-carboxamide | HCID 57682685 | — |
Reaction Steps
To a solution of 1-methyl-5-aminoisoquinoline (94 (75 mg, 0.47 mmol) in DCM (4 ml) was added 4-biphenylcarboxylic acid (141 mg, 0.71 mmol), 1-(3-dimethylaminopropyl)-3-ethyl-carbodiimide hydrochloride (135 mg, 0.71 mmol) and 4-dimethylaminopyridine (10 mg, 0.08 mmol) and the reaction stirred at 38° C. for 3 days. The mixture was diluted with DCM, washed with sat. aqueous sodium bicarbonate solution and water, dried over MgSO4 and concentrated in vacuo to give the crude product which was triturated with methanol. The resulting precipitate was collected by filtration, washed with ether and dried in vacuo giving the title compound as an off-white solid. 1H NMR (400 MHz, CDCl3) δ (ppm): 8.48 (d, 1H), 8.33 (d, 1H), 8.21 (br, 1H), 8.06 (m, 3H), 7.78 (d, 2H), 7.68 (m, 3H), 7.58 (d, 1H), 7.51 (t, 2H), 7.41 (t, 1H), 3.02 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07538121B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-14027445796e482cb578d89752b33991 |
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| Source note | uspto-grants-2009_05 |
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