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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2047163Generated: November 3, 2026

N-methyl-2-pyrrolidone → HCID 67494458, compound

https://huagongshe.com/reaction/2047163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantSodium BicarbonateHCID 516892—
ReactantThiomorpholine 1,1-dioxideHCID 6484228—
Reactant(5-Chloro-3-quinolin-3-yl-pyrazolo[1,5-a]pyrimidin-7-yl)-bis-(2-trimethylsilanyl-ethoxymethyl)-amineHCID 86664780—
SolventWaterHCID 962—
ProductHCID 67494458HCID 67494458—

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 5-chloro-3-(quinolin-3-yl)-N,N-bis((2-(trimethylsilyl)ethoxy)methyl)pyrazolo[1,5-a]pyrimidin-7-amine (503.0 mg, 0.91 mmoL), thiomorpholine 1,1-dioxide (367.1 mg, 2.72 mmoL), NaHCO3 (533.0 mg, 6.34 mmoL) in NMP (8 mL) was heated at 130° C. overnight. The mixture was cooled to room temperature and diluted with H2O and then extracted with ethyl acetate (×2). The combined organic layers were washed with brine and dried with Na2SO4. Evaporation of solvent afforded the crude displacement compound. Purification by column chromatography afforded compound 5-thiomorpholinodioxo-3-(quinolin-3-yl)-N,N-bis((2-(trimethylsilyl)ethoxy)methyl)pyrazolo[1,5-a]pyrimidin-7-amine LCMS tR=2.52 Min (5 min run, UV254nm). Mass calculated for, M+ 654.2, observed m/z 655.2 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08591943B2
Source datasetuspto-grants-2013_11
ORD IDord-fbe7ce9365844e0a92789481c7560a21
Source noteuspto-grants-2013_11