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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768946Generated: October 26, 2026

Piperazine, 1-(1-adamantyl)- → 1-(1-Adamantyl)-4-(2,6-diamino-4-pyrimidinyl)-piperazine

https://huagongshe.com/reaction/1768946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazine, 1-(1-adamantyl)-HCID 35373—
Reactant2,4-Diamino-6-chloropyrimidineHCID 67432—
SolventEthanolHCID 702—
Product1-(1-Adamantyl)-4-(2,6-diamino-4-pyrimidinyl)-piperazineHCID 1894630080.2%

Reaction Conditions

Temperature170 °C

Reaction Steps

A mixture of 2,6-diamino-4-chloropyrimidine (0.43 g, 3.0 mmol) and 1-(1-adamantyl)-piperazine (0.66 g, 3.0 mmol) in ethanol (30 ml) was heated in a sealed tube at 170° C. for 3 hours. After cooling the solvent was removed, the solid residue was dissolved in water (45 ml) and acidified to pH=3 with conc. HCl. The obtained mixture was heated to 50° C. the insolubles were filtered off and the clear solution was rendered alkaline with 10N NaOH under stirring and cooling. The precipitated crystals were collected, washed with water until neutral and dried. In this manner 0.79 g of the title compound was obtained in the form of its monohydrate, yield: 76.6%, mp. 265°-268° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05380724
Source datasetuspto-grants-1995_01
ORD IDord-ffaac1866e2e41fd8560fdae32cb8b29
Source noteuspto-grants-1995_01