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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43071Generated: October 26, 2026

1-Isopropylpiperazine → 2-(4-Isopropyl-piperazin-1-yl)-5-nitro-pyrimidine

https://huagongshe.com/reaction/43071

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IsopropylpiperazineHCID 78013—
Reactant2-Chloro-5-nitropyrimidineHCID 82544—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2-(4-Isopropyl-piperazin-1-yl)-5-nitro-pyrimidineHCID 6691466789.1%

Reaction Conditions

Temperature5 °C

Reaction Steps

1-Isopropyl-piperazine (1.8 mL, 12.7 mmol, 2 equiv) was added to a cold (5° C.) solution of 2-chloro-5-nitropyrimidine (1 g, 6.3 mmol,) in DCM (5 mL). The reaction mixture was stirred for 20 min at 5° C. and then diluted with DCM and H2O. The aqueous layer was separated and extracted with DCM. The organic phase was washed with brine, dried (Na2SO4), filtered and concentrated to provide 1.41 g of the title compound as a beige solid: ESI-MS: 252.2 [M+H]+; tR=1.89 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536175B2
Source datasetuspto-grants-2013_09
ORD IDord-9d3642df068f43569df35b2a9c34155a
Source noteuspto-grants-2013_09