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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366400Generated: October 29, 2026

Chloride → 4-(2,5-dihydro-1H-pyrrol-1-yl)-5-fluoro-6-hydrazino-2-methylpyrimidine

https://huagongshe.com/reaction/1366400

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
ReactantHydrazineHCID 9321—
Reactant3-PyrrolineHCID 66059—
ReactantDiisopropylethylamineHCID 81531—
Reactant4,6-Dichloro-5-fluoro-2-methylpyrimidineHCID 13731033—
SolventDimethyl SulfoxideHCID 679—
SolventMethanolHCID 887—
Product4-(2,5-dihydro-1H-pyrrol-1-yl)-5-fluoro-6-hydrazino-2-methylpyrimidineHCID 6693618768%

Reaction Steps

4,6-Dichloro-5-fluoro-2-methylpyrimidine (181 mg, 1.0 mmol) was dissolved in 4 mL of DMSO and stirred at room temperature. 3-Pyrroline (71 mg, 1.05 mmol) was added, followed by DIPEA (244 μL, 1.4 mmol). The resulting reaction mixture was stirred until displacement of the first chloride was complete, and then hydrazine (350 μL) and MeOH (˜2 mL) were added to the reaction mixture. The contents were then heated to 70° C. for 2 h, until displacement of the second chloride was complete. The reaction mixture was then cooled to room temperature and purified by RP-HPLC to provide 4-(2,5-dihydro-1H-pyrrol-1-yl)-5-fluoro-6-hydrazino-2-methylpyrimidine (142 mg, 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893056B2
Source datasetuspto-grants-2011_02
ORD IDord-cdcfdefa60e540db87cd497d522a6525
Source noteuspto-grants-2011_02