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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219718Generated: October 26, 2026

Lithium Hydroxide → Hydrochloric Acid

https://huagongshe.com/reaction/219718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HydroxideHCID 3939—
ReactantSodium IodideHCID 5238—
Reactant2-tert-Butyl-4-[4-(3-chloro-propyl)-piperazin-1-yl]-6-cyclobutyl-pyrimidineHCID 66673104—
ReactantHCID 178418793HCID 178418793—
SolventDimethylformamideHCID 6228—
ProductHydrochloric AcidHCID 313—
Product2-tert-Butyl-4-cyclobutyl-6-{4-[3-(pyrimidin-2-ylsulfanyl)-propyl]-piperazin-1-yl}-pyrimidine hydrochlorideHCID 69028350—

Reaction Conditions

Temperature60 °C

Reaction Steps

0.4 g of 2-mercapto-pyrimidine (3.57 mmol) were dissolved in 20 ml of dimethylformamide. After addition of 0.09 g of lithium hydroxide (3.57 mmol) and 0.27 g of sodium iodide (1.78 mmol), the reaction mixture was stirred at 60° C. and 1.25 g of 2-tert-butyl-4-[4-(3-chloro-propyl)-piperazin-1-yl]-6-cyclobutyl-pyrimidine (3.57 mmol) were added in portions. The mixture was stirred at 60° C. for 1 h. After cooling, the dimethylformamide was evaporated and the residue was partitioned between 30 ml of ethyl acetate and half-saturated sodium chloride solution (15 ml of saturated aqueous sodium chloride solution and 15 ml of water). The aqueous phase was reextracted twice with ethyl acetate. The combined organic layers were dried over magnesium sulfate, filtered, and concentrated to dryness. The crude product was redissolved in 30 ml of ethyl acetate. The hydrochloride was formed by addition of 4 N hydrochloric acid in dioxane to yield 1.8 g of the title compound as a crystallized hydrochloride salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202868B2
Source datasetuspto-grants-2012_06
ORD IDord-ff387543f4a44429bc000989f0b2b8b1
Source noteuspto-grants-2012_06