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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366475Generated: October 29, 2026

Diisopropylethylamine → HCID 86636952, compound

https://huagongshe.com/reaction/1366475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4,6-Dichloro-5-fluoro-2-methylpyrimidineHCID 13731033—
ReactantHCID 66935961HCID 66935961—
SolventDichloromethaneHCID 6344—
ProductHCID 86636952HCID 86636952118.2%

Reaction Conditions

Temperature35 °C

Reaction Steps

To a solution of (3R)-1,3-dimethylpiperazine dihydrochloride (Example 63) (5.88 g, 31.4 mmol) in dichloromethane (126 mL) was added N,N-diisopropylethylamine (18.11 mL, 104 mmol), and 4,6-dichloro-5-fluoro-2-methylpyrimidine (5.69 g, 31.4 mmol). The solution was heated at 35° C. and stirred for 3 days. The solution was cooled to room temperature, diluted with DCM (100 mL), and washed with sat. aq. NaHCO3 (100 mL). The aqueous phase was extracted with a fresh portion of DCM (50 mL), and the combined organic phase was dried over anhydrous Na2SO4, filtered, and concentrated in vacuo to give crude 4-chloro-6-[(2R)-2,4-dimethyl-1-piperazinyl]-5-fluoro-2-methylpyrimidine (9.60 g, >100% yield) as a brown oil that was used without further purification. LCMS: (M+H)+: 258.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893056B2
Source datasetuspto-grants-2011_02
ORD IDord-95ca18012bfe46068a161c298ea61efd
Source noteuspto-grants-2011_02