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Methyl 3,3-dimethyl-4-pentenoate → 3-Methyl-3-{3-[4-(2-methyl-quinolin-4-ylmethoxy)-phenyl]-4,5-dihydro-isoxazol-5-yl}-butyric acid methyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methyl 3,3-dimethyl-4-pentenoate | HCID 114129 | — |
| 反応物 | 4-(2-Methyl-quinolin-4-ylmethoxy)-benzaldehyde oxime | HCID 73853079 | — |
| 生成物 | 3-Methyl-3-{3-[4-(2-methyl-quinolin-4-ylmethoxy)-phenyl]-4,5-dihydro-isoxazol-5-yl}-butyric acid methyl ester | HCID 69639772 | 100% |
反応手順
Following a procedure analogous to that used in Example step 1c, but using 3,3-dimethyl-pent-4-enoic acid methyl ester 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 3-methyl-3-{3-[4-(2-methyl-quinolin-4-ylmethoxy)-phenyl]-4,5-dihydro-isoxazol-5-yl}-butyric acid methyl ester (0.14 g, 100%) as a crude oil. MS found: (M+H)+=433.
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-b07f9fd71de443e99d9ad915d13ceec6 |
| 出典メモ | uspto-grants-2006_10 |