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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326502Generated: October 30, 2026

4-(Piperazin-1-yl)-2,6-di(pyrrolidin-1-yl)pyrimidine → HCID 69223635, compound

https://huagongshe.com/reaction/326502

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Piperazin-1-yl)-2,6-di(pyrrolidin-1-yl)pyrimidineHCID 14585243—
ReactantHCID 86745586HCID 86745586—
SolventDimethylformamideHCID 6228—
ProductHCID 69223635HCID 69223635—

Reaction Steps

3β-Hydroxy-21-iodo-16α-methylpregn-5-en-20-one (10 g) is added all at once to 4-[2,6-bis(1-pyrrolidinyl)-4-pyrimidinyl]piperazine (16 g) in DMF (400 ml) at 65° and then concentrated to 50 ml under reduced pressure. The concentrate is added to sodium dihydrogen phosphate (0.3M, 400 ml) and ethyl acetate (500 ml). The pH is adjusted to 4.5 with 0.3M phosphoric acid. The ethyl acetate layer is separated and extracted with sodium dihydrogen phosphate (0.3M, 2×200 ml). The ethyl acetate extract is then washed with phosphoric acid (0.3M, 400 ml). The acid extract is stirred and the ph is adjusted to 3.5 with sodium hydroxide (10%). The resulting precipitate is filtered, washed with water (200 ml) and dried to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05268477
Source datasetuspto-grants-1993_12
ORD IDord-849fcf9df5714a9d90cad13d0883e44f
Source noteuspto-grants-1993_12