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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 884656Generated: October 26, 2026

N-(3-Aminopropyl)morpholine → HCID 178422596, compound

https://huagongshe.com/reaction/884656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(3-Aminopropyl)morpholineHCID 61055—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1-(3-(Dimethylamino)propyl)-3-ethylcarbodiimide methiodideHCID 122242—
Reactant({3-[6-(4-Hydroxy-3-methylphenyl)-2-oxo-2,3-dihydropyrimidin-4-yl]phenyl}oxy)acetic acidHCID 178422597—
SolventDimethylformamideHCID 6228—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 178422596HCID 17842259620.9%

Reaction Steps

({3-[6-(4-hydroxy-3-methylphenyl)-2-oxo-2,3-dihydropyrimidin-4-yl]phenyl}-oxy)acetic acid (Compound 222, 17 mg, 48 umol) and 3-morpholinopropan-1-amine (5.8 mg, 40 umol) were dissolved in dichloroethane (1.25 mL) and N,N-dimethylformamide (0.79 mL). To this solution was added 1-hydroxybenzotriazole (6.8 mg, 50 umol) followed by 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide methiodide (17.8 mg, 60 umol). The reaction mixture was stirred at room temperature for 15 hours and was concentrated in vacuo. The reaction mixture was purified by reverse phase HPLC to give 4 mg of product. 1H NMR (400 MHz, d6-DMSO): δ 8.31 (s, 1H), 8.17 (t, 1H), 7.96 (s, 1H), 7.87 (dd, 1H), 7.75 (d, 1H), 7.68 (s, 1H), 7.47 (t, 1H), 7.38 (s, 1H), 7.17 (dd, 1H), 6.92 (d, 1H), 4.61 (s, 2H), 3.61 (t, 4H), 3.21-3.16 (m, 2H), 2.30-2.22 (m, 6H), 2.20 (s, 3H), 1.63-1.57 (m, 2H). MS (EI): 480 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08242129B2
Source datasetuspto-grants-2012_08
ORD IDord-f2c5b2b6c72548798a9f2991c1427a0a
Source noteuspto-grants-2012_08