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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 859805Generated: November 1, 2026

N-(3-Aminopropyl)morpholine → HCID 69152822, compound

https://huagongshe.com/reaction/859805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(3-Aminopropyl)morpholineHCID 61055—
Reactant1-HydroxybenzotriazoleHCID 75771—
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—
Reactant5'-(3-Furoylamino)-2'-methyl-1,1'-biphenyl-4-carboxylic acidHCID 69152146—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 69152822HCID 69152822—

Reaction Steps

5′-(3-Furoylamino)-2′-methyl-1,1′-biphenyl-4-carboxylic acid (50 mg, 0.156 mmol), 4-(3-aminopropyl)morpholine (22.5 mg, 0.156 mmol), HATU (59.2 mg, 0.156 mmol), HOBT (21 mg, 0.156 mmol) and DIPEA (27 μl, 0.156 mmol) in DMF (2 ml) were stirred at room temperature for 18 h. The reaction was diluted with ethyl acetate (150 ml), washed with water (2×30 ml) and dried (magnesium sulphate). The solvent was evaporated under vacuum and the residue chromatographed on a silica flash column eluting with DCM/methanoltriethylamine (96:2:2). Concentration of the product fractions under vacuum N-(6-methyl-4′-{[(3-morpholin-4-ylpropyl)amino]carbonyl}-1,1′-biphenyl-3-yl)-3-furamide (59.5 mg, 83%). NMR; δH [2H6]-DMSO 9.94,(1H, s), 8.55,(1H, t), 8.36,(1H, s), 7.90,(2H, d), 7.78,(1H, t), 7.67,(1H, dd), 7.60,(1H, d), 7.43,(2H, d), 7.27,(1H, d), 6.98,(1H, m), 3.56,(4H, t), 3.30,(2H, m), 2.35–2.32,(6H, m), 2.19,(3H, s), 1.69,(2H, m). LCMS: retention time 2.42 min, MH+448.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07151118B2
Source datasetuspto-grants-2006_12
ORD IDord-a7b9abe874294977bd3a3d7ebf6e8543
Source noteuspto-grants-2006_12