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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 421365Generated: October 26, 2026

N-methyl-2-pyrrolidone → HCID 59333584, compound

https://huagongshe.com/reaction/421365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-2-pyrrolidoneHCID 13387—
Reactant2-Methylpiperazine, (R)-HCID 7330434—
Reactant2-(2-aminopyrimidin-5-yl)-8-chloro-6-(morpholin-4-yl)-9-(2,2,2-trifluoroethyl)-9H-purineHCID 59333534—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 59333584HCID 5933358490.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

An N-methyl-2-pyrrolidone suspension (24 ml) of 5-[8-chloro-6-morpholin-4-yl-9-(2,2,2-trifluoroethyl)-9H-purin-2-yl]pyrimidin-2-amine (2.42 g, 5.82 mmol) and (2R)-2-methylpiperazine (2.92 g, 29.1 mmol) was heated at 120° C. to dissolve and the resulting mixture was stirred at 100° C. for 6 hours. The resulting mixture was left standing to cool, then poured into methylene chloride-methanol (10:1), and washed with water. The organic layer was dried over anhydrous sodium sulfate, the mixture was filtrated, the filtrate was concentrated under reduced pressure, and the resulting residue was purified by medium pressure silica gel column chromatography (methylene chloride:methanol=32:1 to 9:1) to give the title compound (2.51 g, 90%) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08097622B2
Source datasetuspto-grants-2012_01
ORD IDord-4c2d57a47e584c6c82615d76d1bd5ce4
Source noteuspto-grants-2012_01