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Sodium hydroxide tetrahydrofuran → 2-{3-isopropyloxy-5-[(N-methyl) 4-toluenesulfonylaminomethyl]benzoylamino}-5-pyridine carboxylic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium hydroxide tetrahydrofuran | HCID 20445995 | — |
| 反応物 | methyl 2-{3-isopropyloxy-5-[(N-methyl) 4-toluenesulfonylaminomethyl]benzoyl}amino-5-pyridine carboxylate | HCID 58780889 | — |
| 生成物 | 2-{3-isopropyloxy-5-[(N-methyl) 4-toluenesulfonylaminomethyl]benzoylamino}-5-pyridine carboxylic acid | HCID 58780929 | — |
反応手順
Standard ester hydrolysis (2M NaOH/THF), as described in Example A, of methyl 2-{3-isopropyloxy-5-[(N-methyl) 4-toluenesulfonylaminomethyl]benzoyl}amino-5-pyridine carboxylate gave the title compound as a pale yellow solid, 1H NMR δ (d6-DMSO): 1.23 (d, 6H), 2.40 (s, 3H), 2.58 (s, 3H), 4.13 (s, 2H), 4.62–4.72 (m, 1H), 7.70 (s, 1H), 7.41–7.52 (m, 4H), 7.73 (d, 2H), 8.31 (s, 2H), 8.84 (s, 1H), 11.16 (s, 1H) m/z 498 (MH)+, 496 (M−H)−.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07160906B2 |
| 出典データセット | uspto-grants-2007_01 |
| ORD ID | ord-7768c6410252413a8e01fbbe6b351989 |
| 出典メモ | uspto-grants-2007_01 |