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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1008842생성일: 2026년 10월 25일

Triethylamine → {6-[4-(Methanesulfonylamino-methyl)-phenyl]-pyridin-2-yl}carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1008842

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methanesulfonyl chlorideHCID 31297—
반응물[6-(4-Aminomethyl-phenyl)-pyridin-2-yl]-carbamic acid tert-butyl esterHCID 59166138—
용매DichloromethaneHCID 6344—
생성물{6-[4-(Methanesulfonylamino-methyl)-phenyl]-pyridin-2-yl}carbamic acid tert-butyl esterHCID 5916593355.8%

반응 단계

To a solution of [6-(4-aminomethyl-phenyl)-pyridin-2-yl]-carbamic acid tert-butyl ester (5.7 g 19 mmol) and Et3N (2.88 g, 29 mmol) in dichloromethane (50 mL) was added dropwise MsCl (2.7 g, 19 mmol) at 0° C. The reaction mixture was stirred at this temperature for 30 min, and then washed with water and brine, dried over Na2SO4 and concentrated to dryness. The residue was recrystallized with DCM/Petroleum Ether (1:3) to give {6-[4-(methanesulfonylamino-methyl)-phenyl]-pyridin-2-yl}carbamic acid tert-butyl ester (4.0 g, 44% over two steps). 1H NMR (300 MHz, CDCl3) δ 7.90-7.97 (m, 3 H), 7.75 (t, J=8.4, 8.4 Hz, 1 H), 7.54-7.59 (m, 1 H), 7.38-7.44 (m, 3 H), 4.73 (br, 1 H), 4.37 (d, J=6.0 Hz, 2 H), 2.90 (s, 3 H), 1.54 (s, 9 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07973038B2
출처 데이터셋uspto-grants-2011_07
ORD IDord-1a74b7563889429e813ef7535263d5db
출처 메모uspto-grants-2011_07