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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711216Generated: October 30, 2026

(1,1'-Biphenyl)-4-carboxylic acid → N-(4-(pyridazin-4-yl)benzyl)biphenyl-4-carboxamide

https://huagongshe.com/reaction/711216

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1,1'-Biphenyl)-4-carboxylic acidHCID 66724—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant(4-(Pyridazin-4-yl)phenyl)methanamineHCID 67208670—
SolventDimethyl SulfoxideHCID 679—
SolventDimethylformamideHCID 6228—
ProductN-(4-(pyridazin-4-yl)benzyl)biphenyl-4-carboxamideHCID 56597948—

Reaction Steps

To a mixture of (4-(pyridazin-4-yl)phenyl)methanamine 1-3 (19 mg, 0.1 mmol), biphenyl-4-carboxylic acid 1-4 (20 mg, 0.1 mmol) and O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluroniumhexafluorophosphate (HATU) (38 mg, 0.1 mmol) in DMF (0.5 mL) was added DIEA (0.052 mL, 0.3 mmol) at room temperature. The mixture was stirred at room temperature for 2 hours. The reaction mixture was diluted into DMSO and purified by HPLC to give N-(4-(pyridazin-4-yl)benzyl)biphenyl-4-carboxamide 1 as a white solid. MS m/z 366.2 (M+1). 1H NMR 400 MHz (DMSO-d6) δ9.59 (m, 1H), 9.21 (dd, 1H), 9.16 (t, 1H), 7.96 (m, 3H), 7.87 (d, 2H), 7.74 (d, 2H), 7.69 (m, 2H), 7.47-7.41 (m, 4H), 7.37 (m, 1H), 4.52 (d, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181235B2
Source datasetuspto-grants-2015_11
ORD IDord-fb5d7c9c48684c9c8dfcff7bc5e6a7d4
Source noteuspto-grants-2015_11