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HRID 1245392作成日:2026年10月27日

Acrolein dimethyl acetal → 4-[4-(5-Dimethoxymethyl-4,5-dihydro-isoxazol-3-yl)-phenoxymethyl]-2-methyl-quinoline

https://huagongshe.com/reaction/1245392

反応式

関与物質

役割名称HCID仕込み量
反応物Acrolein dimethyl acetalHCID 80145—
反応物4-(2-Methyl-quinolin-4-ylmethoxy)-benzaldehyde oximeHCID 73853079—
生成物4-[4-(5-Dimethoxymethyl-4,5-dihydro-isoxazol-3-yl)-phenoxymethyl]-2-methyl-quinolineHCID 21911177100%

反応手順

Following a procedure analogous to that used in Example step 1c, but using 3,3-dimethoxy-propene and 4-(2-methyl-quinolin-4-ylmethoxy)-benzaldehyde oxime from step 1b, the crude reaction was partitioned between ethyl acetate and water and the organic layer was washed with brine, dried over magnesium sulfate, and concentrated to give 4-[4-(5-dimethoxymethyl-4,5-dihydro-isoxazol-3-yl)-phenoxymethyl]-2-methyl-quinoline (0.4 g, 100%) as a crude oil. MS found: (M+H)+=393.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07125870B2
出典データセットuspto-grants-2006_10
ORD IDord-4924a64531f34706a08014fded8fd5f9
出典メモuspto-grants-2006_10