HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220112Generated: October 29, 2026
2-(1-Piperidyl)ethoxyamine dihydrochloride → 4-(3-Chloro-4-(3-fluorobenzyloxy)phenylamino)-6-(2-(1-piperidyl)ethoxyimino)quinazoline
https://huagongshe.com/reaction/220112
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(1-Piperidyl)ethoxyamine dihydrochloride | HCID 21275674 | — |
| Reactant | 4-(3-Chloro-4-(3-fluorobenzyloxy)phenylamino) 6-formylquinazoline | HCID 57733656 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(3-Chloro-4-(3-fluorobenzyloxy)phenylamino)-6-(2-(1-piperidyl)ethoxyimino)quinazoline | HCID 86630915 | 20.3% |
Reaction Steps
In a mixture of tetrahydrofuran (2 ml) and water (0.1 ml) were dissolved 4-(3-chloro-4-(3-fluorobenzyloxy)phenylamino)-6-formylquinazoline (IV-1, 50 mg) and 2-(1-piperidyl)ethoxyamine dihydrochloride (36.5 mg), and the mixture was stirred at room temperature overnight. The reaction mixture was diluted with ethyl acetate, washed sequentially with aqueous saturated sodium bicarbonate solution, and aqueous sodium chloride solution, and dried over magnesium sulfate. After concentration, the residue was purified by chromatography (eluting with hexane:ethyl acetate=2:3) using an amino column, and further re-purified by thin layer chromatography to obtain 4-(3-chloro-4-(3-fluorobenzyloxy)phenylamino)-6-(2-(1-piperidyl)ethoxyimino)quinazoline (V-1, 13 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08202879B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-48c75bf2b9d8478e9c8c418bf796efd7 |
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| Source note | uspto-grants-2012_06 |
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