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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219711Generated: October 30, 2026

Sodium Iodide → Acetic acid 3-[4-(2-tert-butyl-6-cyclopropyl-pyrimidin-4-yl)-piperazin-1-yl]-propyl ester

https://huagongshe.com/reaction/219711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantTriethylamineHCID 8471—
Reactant1-Propanol, 3-chloro-, acetateHCID 12334—
Reactant2-Tert-butyl-4-piperazin-1-yl-6-cyclopropyl-pyrimidineHCID 67372611—
SolventDimethylformamideHCID 6228—
ProductAcetic acid 3-[4-(2-tert-butyl-6-cyclopropyl-pyrimidin-4-yl)-piperazin-1-yl]-propyl esterHCID 69026905—

Reaction Conditions

Temperature80 °C

Reaction Steps

2.9 g of 2-tert-Butyl-4-piperazin-1-yl-6-cyclopropyl-pyrimidine (11.1 mmol), 1.8 g acetic acid 3-chloro-propyl ester (13.2 mmol), 1.38 g of triethylamine (13.7 mmol), and a spatula tip of sodium iodide were dissolved in 50 ml of dimethylformamide and stirred for 8 h at 80° C. After cooling to room temperature, the dimethylformamide was evaporated. The reaction mixture was partitioned between water and ethyl acetate. The organic layer was dried over magnesium sulfate, filtered, and the solvent was evaporated. The crude product (3.7 g) was directly used in the subsequent reaction step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202868B2
Source datasetuspto-grants-2012_06
ORD IDord-184b0733e8444260864a6e980e6ad5c3
Source noteuspto-grants-2012_06