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Triethylamine hydrochloride → 1-(2-hydroxy-3-propyl-4-{3-[4-(2H-tetrazol-5-yl)-pyridin-2-ylsulfanyl]-benzyloxy}-phenyl)-ethanone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine hydrochloride | HCID 11130 | — |
| 反応物 | Sodium Azide | HCID 33557 | — |
| 反応物 | 2-(3-((4-Acetyl-3-hydroxy-2-propylphenoxy)methyl)phenylthio) isonicotinonitrile | HCID 68535659 | — |
| 生成物 | 1-(2-hydroxy-3-propyl-4-{3-[4-(2H-tetrazol-5-yl)-pyridin-2-ylsulfanyl]-benzyloxy}-phenyl)-ethanone | HCID 59599572 | — |
反応手順
Employing the procedure essentially as described in Example 1 using 2-[3-(4-acetyl-3-hydroxy-2-propyl-phenoxymethyl)-phenylsulfanyl]-isonicotinonitrile (380 mg, 0.908 mmol), sodium azide (590 mg, 9.08 mmol), and triethylamine hydrochloride (1.25 g, 9.08 mmol), the title compound is obtained as a white solid (261 mg, 62%): 1H NMR (DMSO-d6) δ 0.760 (t, 3H), 1.39 (sextuplet, 2H), 2.52 (t, 2H), 2.56 (s, 3H), 5.32 (s, 2H), 6.71 (d, 1H), 7.59 (m, 4H), 7.73 (m, 2H), 7.79 (d, 1H), 8.64 (d, 1H), 12.82 (s, 1H); MS (esi negative) m/z 460 (m−1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07858646B2 |
| 出典データセット | uspto-grants-2010_12 |
| ORD ID | ord-30d6854ae7964fc5bdc621314bf9741d |
| 出典メモ | uspto-grants-2010_12 |