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Pyridine-2-sulfonyl chloride hydrochloride → HCID 54361077、化合物
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Pyridine-2-sulfonyl chloride hydrochloride | HCID 13791306 | — |
| 反応物 | 3-{3-[(4-Pyridin-3-yl-benzylamino)-methyl]-phenyl}-propionic acid methyl ester | HCID 54243195 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 生成物 | HCID 54361077 | HCID 54361077 | — |
反応手順
The title compound of Step A was prepared from 3-{3-[(4-pyridin-3-yl-benzylamino)-methyl]-phenyl}-propionic acid methyl ester, prepared in Step A of Example 11m, and pyridine-2-sulfonyl chloride hydrochloride, of Preparation 47, following the method described in Example 1, Step B using triethylamine in place of N,N-diisopropylethylamine. 1 H NMR (400 MHz, CDCl3) δ 8.79 (s, 1H), 8.69 (d, 1H), 8.59 (d, 1H), 7.98 (m, 1H), 7.88 (m, 2H), 7.49-7.38 (m, 4H), 7.24 (m, 2H), 7.11 (m, 1H), 7.02 (d, 1H), 6.95 (d, 1H), 6.90 (s, 1H), 4.54 (s, 2H), 4.49 (s, 2H), 3.65 (s, 3H), 2.80 (t, 2H), 2.49 (t, 2H); MS 502 (M+1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07442702B2 |
| 出典データセット | uspto-grants-2008_10 |
| ORD ID | ord-021cd1996bc040529f57b73261cb3ac4 |
| 出典メモ | uspto-grants-2008_10 |