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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109913Generated: October 28, 2026

1-Methylpiperazine → HCID 3252419, compound

https://huagongshe.com/reaction/1109913

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
Reactant2,4,5-TrichloropyrimidineHCID 237259—
SolventEthanolHCID 702—
ProductHCID 3252419HCID 3252419—

Reaction Steps

Trichloropyrimidine is added in portions to an ice cool solution of N-methylpiperazine (40 g) in ethanol (200 ml). The mixture is then heated at 60° for 2 h. The mixture is concentrated and chromatographed on silica gel with 2-5% methanol and methylene chloride to give 2,4-bis[4-methylpiperazino]-6-chloropyrimidine. This material is heated at 130° in water (30 ml) with piperazine (32 g) in a Parr bomb for 20 h. The product is partitioned between methylene chloride and aqueous sodium carbonate. The phases are separated and the organic phase is dried over sodium sulfate and concentrated to give the title compound, TLC (methylene chloride/methanol/ammonium hydroxide - 91.5/8/0.5) Rf =0.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05322943
Source datasetuspto-grants-1994_06
ORD IDord-75592be042584991aea625099a2026e5
Source noteuspto-grants-1994_06