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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426401Generated: October 30, 2026

Sodium Iodide → Benzyl 4-(pyrimidin-4-yl-methyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1426401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantDiisopropylethylamineHCID 81531—
ReactantN-Cbz-N,N-bis(2-chloroethyl)amineHCID 12553191—
ReactantPyrimidin-4-ylmethanamineHCID 12933348—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
SolventDiglymeHCID 8150—
ProductBenzyl 4-(pyrimidin-4-yl-methyl)piperazine-1-carboxylateHCID 67518105—

Reaction Conditions

Temperature150 °C

Reaction Steps

To a stirred solution of 0.20 g (1.8 mmol) of 1-(pyrimidin-4-yl)methanamine and 0.61 g (2.2 mmol) benzyl bis(2-chloroethyl)carbamate in 4 mL anhydrous diethylene glycol dimethyl ether was added 3.20 mL (18.3 mmol) of N,N-diisopropylethylamine and 0.05 g (0.40 mmol) of sodium iodide. The resulting solution was heated to 150° C. for 6 h. After cooling to ambient temperature, 12 mL of methanol was added to the mixture followed by 250 mL of diethyl ether. The resulting white precipitate was isolated by vacuum filtration while washing with diethyl ether. Diluted the solid with 100 mL of saturated sodium bicarbonate and extracted the aqueous solution with ethyl acetate (3×100 mL). The combined organic layers were dried with magnesium sulfate, filtered, and concentrated in vacuo to afford the title compound as a white solid which was used without further purification. LC/MS: m/z (ES) 313.1 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933102B2
Source datasetuspto-grants-2015_01
ORD IDord-4edd9be00ff041d19ba558728d4aa539
Source noteuspto-grants-2015_01