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Acrolein dimethyl acetal → 4-[4-(5-Dimethoxymethyl-4,5-dihydro-isoxazol-3-yl)-phenoxymethyl]-2-methyl-quinoline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acrolein dimethyl acetal | HCID 80145 | — |
| 反応物 | 4-(2-Methyl-quinolin-4-ylmethoxy)-benzaldehyde oxime | HCID 73853079 | — |
| 生成物 | 4-[4-(5-Dimethoxymethyl-4,5-dihydro-isoxazol-3-yl)-phenoxymethyl]-2-methyl-quinoline | HCID 21911177 | 100% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07125870B2 |
| 出典データセット | uspto-grants-2006_10 |
| ORD ID | ord-4924a64531f34706a08014fded8fd5f9 |
| 出典メモ | uspto-grants-2006_10 |