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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044651Generated: October 25, 2026

Water → HCID 44250837, compound

https://huagongshe.com/reaction/1044651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium NitriteHCID 23668193—
Reactant4,6-Dimorpholino-2-(4-phenylpiperazin-1-yl)pyrimidineHCID 44250437—
SolventAcetic AcidHCID 176—
ProductHCID 44250837HCID 4425083752.4%

Reaction Steps

The synthesis method shall be explained concretely, and in order, below. 4,6-dimorpholino-2-(4-phenylpiperazin-1-yl)pyrimidine (3.0 g, 7.31 mmol) was dissolved in acetic acid (20 ml), an aqueous solution (1 ml) of sodium nitrite (605 mg, 8.78 mmol) was dripped in under water cooling, and agitation was done for 30 minutes at room temperature. After adjusting the pH to approximately 4.0 with a 2N NaOH aqueous solution, extraction was carried out 2 times using dichloromethane. After washing with water, drying was done with MgSO4, and the solvent was distilled away under reduced pressure. The residue was dissolved in a methanol (40 ml)-ethyl acetate (40 ml) mixture solvent, 300 mg of Pd/C was added, and catalytic hydrogenation was done for 2 hours under atmospheric pressure. The Pd/C was filtered using celite, and the filtered liquid was distilled away under reduced pressure. The residue was washed with ether, and 1.63 g (52% yield) of 5-amino-4,6-dimorpholino-2-(4-phenylpiperazin-1-yl)pyrimidine was obtained. The melting point measurement result, the MS measurement result, and the NMR data for the obtained Compound 63 are shown below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563715B2
Source datasetuspto-grants-2013_10
ORD IDord-42354e392de14dcda13a6bf5fa0189bd
Source noteuspto-grants-2013_10