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4-Methyl-alpha-(4-methylphenyl)benzeneacetic acid → N-{5-[1-(3-{[Bis(4-methylphenyl)acetyl]amino}propyl)4-piperidinyl]-2-fluorophenyl}butanamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Methyl-alpha-(4-methylphenyl)benzeneacetic acid | HCID 30314 | — |
| 反応物 | N-{5-[1-(3-aminopropyl)4-piperidinyl]-2-fluorophenyl}butanamide | HCID 21957132 | — |
| 生成物 | N-{5-[1-(3-{[Bis(4-methylphenyl)acetyl]amino}propyl)4-piperidinyl]-2-fluorophenyl}butanamide | HCID 21957134 | — |
反応手順
Example 109 was prepared from bis(4-methylphenyl)acetic acid and N-{5-[1-(3-aminopropyl)-4-piperidinyl]-2-fluorophenyl}butanamide according to the procedures described in Scheme 10: 1H NMR (400 MHz, CDCl3) δ 8.30–8.13 (m, 1H), 8.08–7.92 (br, 1H), 7.43–6.89 (m, 9H), 6.76–6.61 (br, 1H), 4.98–4.79 (br, 1H), 4.70 (s, 1H), 3.39–3.16 (m, 4H), 2.83–2.63 (m, 2H), 2.63–2.47 (m, 1H), 2.45–2.12 (m, 4H), 2.27 (s, 6H), 2.02–1.64 (m, 8H), 1.02 (t, 3H, J=7.2 Hz); ESMS m/e: 544.4 (M+H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07105544B2 |
| 出典データセット | uspto-grants-2006_09 |
| ORD ID | ord-7b4adabf4ced4a17a8e4afc66640601a |
| 出典メモ | uspto-grants-2006_09 |