돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2180445생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/2180445

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methyl 6-aminohexanoate hydrochlorideHCID 11499324—
반응물Pyridine-3-sulfonyl chloride hydrochlorideHCID 12571517—
용매AcetonitrileHCID 6342—
생성물6-(Pyridine-3-sulfonylamino)hexanoic acid methyl esterHCID 2078048976.1%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06888027B2
출처 데이터셋uspto-grants-2005_05
ORD IDord-dce5aa16e0924a708609dc37d6e30950
출처 메모uspto-grants-2005_05