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3,4-diamino-N-(4-tert-butylphenyl)-benzamide → (3-{4-[6-(4-tert-Butyl-phenylcarbamoyl)-1H-benzoimidazol-2-yl]-3,5-dimethyl-phenyl}-propyl)-phosphonic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3,4-diamino-N-(4-tert-butylphenyl)-benzamide | HCID 66966111 | — |
| 反応物 | [(E)-3-(4-formyl-3,5-dimethylphenyl)-allyl]-phosphonic acid diethyl ester | HCID 86632823 | — |
| 生成物 | (3-{4-[6-(4-tert-Butyl-phenylcarbamoyl)-1H-benzoimidazol-2-yl]-3,5-dimethyl-phenyl}-propyl)-phosphonic acid | HCID 66966068 | — |
反応手順
The title compound was prepared from 3,4-diamino-N-(4-tert-butylphenyl)-benzamide (from Example 6-26) and [(E)-3-(4-formyl-3,5-dimethylphenyl)-allyl]-phosphonic acid diethyl ester analogous to Example 6-32. 1H NMR (Methanol-d4, 400 MHz): δ 8.25 (dd, 1H), 7.92 (dd, 1H), 7.72 (dd, 1H), 7.63 (m, 2H), 7.42 (m, 2H), 7.06 (s, 2H), 2.73 (t, 2H), 2.14 (s, 6H), 1.95 (m, 2H), 1.69 (m, 2H), 1.33 (s, 9H). MS (m/z) 520.2 (M+1); Retention time: 1.19 min (Method 10).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08222248B2 |
| 出典データセット | uspto-grants-2012_07 |
| ORD ID | ord-16df952a5dad484087f9b3cb70f98fb6 |
| 出典メモ | uspto-grants-2012_07 |