関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Lithium diisopropylamide | HCID 2724682 | — |
| 反応物 | 9-hydroxy-4-iodopyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione | HCID 11842834 | — |
| 反応物 | (2-Chloro-5-methoxybenzyl)(triphenyl)phosphonium bromide | HCID 85758264 | — |
| 生成物 | 2-[(E)-2-(2-chloro-5-methoxyphenyl)ethenyl]-5-methoxy-1H-indole | HCID 11844220 | — |
反応手順
The 5-methoxy-1H-indole-2-carbaldehyde (1) was reacted with (2-chloro-5-methoxybenzyl)(triphenyl)phosphonium bromide (578) prepared as described in example 166 using the procedure described in example 37, except that the LDA and aldehyde were (sequentially) added at 0° C., the ratio of LDA:aldehyde was 1.5:1 and the reaction time was 5 h, to give (after crystallisation from CH2Cl2/hexane) the diene (579) as a pale yellow solid (the pure E isomer) (85%), mp 119–121° C. 1H NMR (CDCl3) δ 8.22 (br s, 1H), 7.29 (d, J=8.9 Hz, 1H), 7.26 (br d, J=8.7 Hz, 1H), 7.22 (d, J=16.5 Hz, 1H), 7.18 (d, J=3.0 Hz, 1H), 7.06 (d, J=16.7 Hz, 1H), 7.04 (br s, 1H), 6.88 (dd, J=8.7, 2.5 Hz, 1H), 6.77 (dd, J=8.8, 3.0 Hz, 1H), 6.59 (d, J=1.8 Hz, 1H), 3.86 (s, 3H), 3.85 (s, 3H). Found: C, 68.70; H, 5.11; N, 4.37. C18H16ClNO2 requires C, 68.90; H, 5.14; N, 4.46.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07094798B1 |
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| 出典データセット | uspto-grants-2006_08 |
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| ORD ID | ord-75df05aa2dc442c2a14c9e3dbed3c708 |
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| 出典メモ | uspto-grants-2006_08 |
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