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
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Thiomorpholine 1,1-dioxide | HCID 6484228 | — |
| Reactant | (5-Chloro-3-quinolin-3-yl-pyrazolo[1,5-a]pyrimidin-7-yl)-bis-(2-trimethylsilanyl-ethoxymethyl)-amine | HCID 86664780 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 67494458 | HCID 67494458 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08591943B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-fbe7ce9365844e0a92789481c7560a21 |
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| Source note | uspto-grants-2013_11 |
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