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N-Allylaniline → 3-(4-Chlorophenyl)-3-(1H-imidazol-1-ylmethyl)-2-methyl-5-[(phenylamino)methyl]isoxazolidine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | N-Allylaniline | HCID 68525 | — |
| 反応物 | 1-(4-chlorophenyl)-2-(1H-imidazol-1-yl)-N-methylethanimine N-oxide | HCID 72727174 | — |
| 生成物 | 3-(4-Chlorophenyl)-3-(1H-imidazol-1-ylmethyl)-2-methyl-5-[(phenylamino)methyl]isoxazolidine | HCID 14234331 | — |
反応手順
Derivative 3 (R1 =4-Cl, R2 =R3 =H) is obtained by a procedure similar to that described in Example 1 by reacting 1-(4-chlorophenyl)-2-(1H-imidazol-1-yl)-N-methylethanimine N-oxide (1: R1 =4-Cl) with N-phenyl-2-propen-1-amine (2: R2 =R3 =H). The product cis-/trans-diastereometric mixture is flash-chromatographed on neutral silica gel using chloroform-methanol (97:3 by volume) as eluent. Isomer A has a melting point of 159°-160° C. (ethyl acetate). Anal. Calcd for C21H23ClN4O: C, 65.87; H, 6.05; N, 14.63; Cl, 9.26. Found: C, 65.77; H, 6.20; N, 14.42; Cl, 9.48. Isomer B has a melting point of 172°-173° C. (ethyl acetate).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04767868 |
| 出典データセット | uspto-grants-1988_08 |
| ORD ID | ord-92bd0a9e9672482cb22f8354e7f581da |
| 出典メモ | uspto-grants-1988_08 |