돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 507360생성일: 2026년 10월 25일

Pyridine → N-(2-methyl-benzooxazol-5-yl)-4-propyl-benzenesulfonamide

https://huagongshe.com/reaction/507360

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Sodium BicarbonateHCID 516892—
반응물2-Methyl-1,3-benzoxazol-5-amineHCID 737920—
반응물4-N-Propylbenzenesulphonyl chlorideHCID 2737222—
용매DichloromethaneHCID 6344—
생성물N-(2-methyl-benzooxazol-5-yl)-4-propyl-benzenesulfonamideHCID 1172418785%

반응 단계

To a solution of 4n-propylbenzenesulphonyl chloride (93 mg, 0.43 mmol) in dichloromethane (2 mL) was added pyridine (80 μL, 1.0 mmol) and the mixture was stirred under N2 for 5 min, after which time 5-amino-2-methylbenzoxazole (60 mg, 0.40 mmol) was added. The resulting mixture was stirred for 1 h at room temperature, then saturated NaHCO3 solution was added (8 mL) and the mixture was extracted into ethyl acetate (15 mL). The organic phase was washed with brine, dried (Na2SO4), filtered and evaporated to give a residue that was purified using flash chromatography to afford a pale pink oil (112 mg, 85%), single spot at Rf 0.53 (1:1 hexane:ethyl acetate). HPLC purity 99+% (tR 2.38 min in 10% water-acetonitrile) 1H NMR (CDCl3): δ 7.64 (2H, dt, J=8.1, 1.8 Hz), 7.31 (2H, m), 7.18 (2H, d, J=8.4 Hz), 7.06 (1H, dd, J=8.6, 2.4 Hz), 2.59 (5H, m), 1.58 (2H, sextet, J=7.3 Hz), 0.89 (3H, t, J=7.3 Hz). LCMS: 329.15 (M−). FAB-MS (MH+, C17H18N2O3S): calcd 331.1116, found 331.1118.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07786152B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-92b4d1a63e984be0b51eb5ff4aa27789
출처 메모uspto-grants-2010_08