戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 351094作成日:2026年10月27日

Triethylamine → 6-(Pyridine-3-sulfonylamino)hexanoic acid methyl ester

https://huagongshe.com/reaction/351094

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Methyl 6-aminohexanoate hydrochlorideHCID 11499324—
反応物Pyridine-3-sulfonyl chloride hydrochlorideHCID 12571517—
溶媒AcetonitrileHCID 6342—
生成物6-(Pyridine-3-sulfonylamino)hexanoic acid methyl esterHCID 2078048976.1%

反応手順

Pyridine-3-sulfonyl chloride hydrochloride (92c) (1.8 g, 5.0 mmol) was added to a solution of methyl 6-aminohexanoate hydrochloride (91) (1.82 g, 10 mmol) and triethylamine (3.03 g, 30 mmol) in acetonitrile (30 ml). The mixture was stirred for 1 hour at ambient temperature, filtered and solvents were removed under reduced pressure. The oily product was dissolved in water (15 ml) and extracted with ethyl ether (50 ml). The extract was dried (Na2SO4) and the solvents were removed under reduced pressure. The title compound (1.09 g, 76%) was obtained as oil and was used for the next step without an additional purification. 1H NMR δH (90 MHz, DMSO-d6) δ: 0.80–1.51 (6H, m, CH2); 1.83 (2H, t, J=6.5 Hz, CH2); 2.76 (2H, t, J=6.5 Hz, CH2N); 3.58 (3H, s, CH3); 7.54 (1H, dd, J=5.0 Hz, J=8.2 Hz, C5HN); 8.12 (1H, dt, J=2.0 Hz, J=8.2 Hz, C5HN); 8.61 (1H, dd, J=2.0 Hz, J=5.0 Hz, C5HN); 8.81 (1H, d, J=2.0 Hz, C5HN).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07183298B2
出典データセットuspto-grants-2007_02
ORD IDord-133fc99d50ea4e698a1a76b5839a0204
出典メモuspto-grants-2007_02