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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102814Generated: November 1, 2026

1-Methylpiperazine → 2-Chloro-4-(4-methylpiperazin-1-yl)pyrimidine

https://huagongshe.com/reaction/2102814

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
Reactant2,4-DichloropyrimidineHCID 77531—
ReactantDiisopropylethylamineHCID 81531—
SolventEthanolHCID 702—
Product2-Chloro-4-(4-methylpiperazin-1-yl)pyrimidineHCID 1714225—

Reaction Conditions

Temperature-10 °C

Reaction Steps

A mixture of 2,4-dichloropyrimidine (0.967 g, 6.49 mmol), 1-methylpiperazine (0.65 g, 6.40 mmol), and ethyldiisopropylamine (2.8 mL, 16.22 mmol) in ethanol (13 mL) was stirred at −10° C. for 2 h and then at r.t. overnight. The mixture was partitioned between H2O/brine (3:1; 100 mL) and chloroform (3×70 mL). The combined organic phases were washed once with brine (50 mL) an dried over MgSO4. Removal of solvent yielded a pale-beige solid, which was washed with ethyl acetate/ultrasound to give the desired product as a colourless powder, which was further washed with Et2O. Additional product was obtained upon fractional crystallization of the washing solution. A total of 0.741 g (3.48 mmol, 54%) of 2-chloro-4-(4-methylpiperazin1-yl)pyrimidine was obtained. LC/ESI-MS: m/z=213 [M(35Cl)+H]+; Rt=0.5 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576090B2
Source datasetuspto-grants-2009_08
ORD IDord-0a7a888992884338845f625d16b2ee58
Source noteuspto-grants-2009_08