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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 23789생성일: 2026년 10월 25일

Triethylamine → {3-[(Pyridine-3-sulfonylamino)-methyl]-phenoxy}-acetic acid tert-butyl ester

https://huagongshe.com/reaction/23789

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Pyridine-3-sulfonyl chloride hydrochlorideHCID 12571517—
반응물t-Butyl [3-(aminomethyl)phenoxy]acetateHCID 20758042—
용매DichloromethaneHCID 6344—
생성물{3-[(Pyridine-3-sulfonylamino)-methyl]-phenoxy}-acetic acid tert-butyl esterHCID 6973062678.1%

반응 단계

To a solution of (3-aminomethyl-phenoxy)-acetic acid tert-butyl ester (296 mg, 1.25 mmol) in CH2Cl2 at 0° C. was added pyridine-3-sulfonyl chloride hydrochloride (279 mg, 1.31 mmol) followed by Et3N (0.36 mL, 2.6 mmol). The reaction was stirred at room temperature for 24 h and was quenched with a 1:1 solution of water and saturated aqueous NaHCO3. The aqueous solution was washed with CH2Cl2 (3×). The combined organic solutions were dried (MgSO4), filtered, and concentrated. Medium pressure chromatography (1:1 hexanes:EtOAc) provided the title compound as a white solid (369.5 mg). 1H NMR (400 MHz, CDCl3) δ 9.04 (s, 1H), 8.75 (m, 1H), 8.09 (d, 1H), 7.44 (m, 1H), 7.15 (m, 1H), 6.76 (m, 3H), 5.23 (bs, 1H), 4.44 (s, 2H), 4.16 (d, 2H), 1.47 (s, 9H); MS 379 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06852863B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-5cb1ec306f794ff79bb04c0138d04ff3
출처 메모uspto-grants-2005_02