HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977142Generated: October 29, 2026
Dimethyl Sulfoxide → 1-ethyl-N-[4-[2-(4-morpholinyl)ethoxy]phenylmethyl]-1H-pyrazolo[3,4-b]quinolin-4-amine
https://huagongshe.com/reaction/977142
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | [4-(2-Morpholinoethoxy)phenyl]methylamine | HCID 7164631 | — |
| Reactant | 1-ethyl-4-chloro-1H-pyrazolo[3,4-b]quinoline | HCID 15816908 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-ethyl-N-[4-[2-(4-morpholinyl)ethoxy]phenylmethyl]-1H-pyrazolo[3,4-b]quinolin-4-amine | HCID 22097534 | 77.2% |
Reaction Steps
A mixture of 1-ethyl-4-chloro-1H-pyrazolo[3,4-b]quinoline (0.7 g, 3 mmol), 4-[2-(4-morpholinyl)ethoxy]phenylmethylamine (0.75 g, 3.2 mmol) and DMSO (3 mL) was heated on a steam bath for 8 hours. Additional 1-ethyl-4-chloro-1H-pyrazolo[3,4-b]quinoline (0.7 g, 3 mmol) was then added and the reaction mixture was heated on a steam bath for another 4 hours. The reaction mixture was cooled to room temperature and then was poured into water. The mixture was extracted with CH2Cl2 (3×100 mL) and then CH2Cl2 layers were combined, dried over MgSO4 and evaporated to dryness. The residue was purified by column chromatography on silica gel eluting with CH2Cl2 /methanol (95/5), followed by recrystallization from ethyl acetate, to afford 1.0 g of 1-ethyl-N-[4-[2-(4-morpholinyl) ethoxy]phenylmethyl]-1H-pyrazolo[3,4-b]quinolin-4-amine, as a yellow solid, m.p. 170°-172° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05614530 |
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| Source dataset | uspto-grants-1997_03 |
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| ORD ID | ord-51718b63e6cd4330b58a086308496109 |
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| Source note | uspto-grants-1997_03 |
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