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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494243Generated: October 26, 2026

7-Aminoquinoline → 3-Methyl-N-quinolin-7-yl-1,1'biphenyl-4-carboxamide

https://huagongshe.com/reaction/494243

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-AminoquinolineHCID 11377—
Reactant3-Methyl-[1,1'-biphenyl]-4-carboxylic acidHCID 14090570—
Product3-Methyl-N-quinolin-7-yl-1,1'biphenyl-4-carboxamideHCID 57682750—

Reaction Steps

Using the procedure outlined in Example 56, the title compound was prepared from 7-aminoquinoline (D55) (31, 0.22 mmol) and 3-methyl-1,1′-biphenyl-4-carboxylic acid (D58) (55 mg, 0.26 mmol) as an off-white solid. 1H NMR (400 MHz, CDCl3) δ (ppm): 8.91(dd, 1H), 8.14 (m, 3H), 7.86 (d, 1H), 7.78 (br, 1H), 7.66 (d, 1H), 7.62 (d, 2H), 7.53 (m, 2H), 7.48 (t, 2H), 7.40 (t, 1H), 7.36 (dd, 1H), 2.63 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538121B2
Source datasetuspto-grants-2009_05
ORD IDord-b12b87bceaaa43da960f1c4274306f1c
Source noteuspto-grants-2009_05