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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1056244생성일: 2026년 10월 26일

Methanesulfonyl chloride → 5-Chloro-2-methylpyrido[3,4-b]pyrazin-3-yl methanesulfonate

https://huagongshe.com/reaction/1056244

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonyl chlorideHCID 31297—
반응물DiisopropylethylamineHCID 81531—
반응물HCID 178432270HCID 178432270—
용매DichloromethaneHCID 6344—
생성물5-Chloro-2-methylpyrido[3,4-b]pyrazin-3-yl methanesulfonateHCID 8978203264%

반응 단계

A solution of 5-chloro-2-methylpyrido[3,4-b]pyrazin-3-ol (1.88 g, 9.61 mmol) in DCM (30 mL) at 0° C. was treated with DIEA (3.34 mL, 19.22 mmol) followed by methanesulfonyl chloride (1.11 mL, 14.42 mmol) (Sigma Aldich). The reaction mixture was warmed to RT and stiffed for 1 h. The mixture was diluted with DCM and washed with water. The organic layer was dried (MgSO4), filtered and concentrated in vacuo. The residue was purified on a silica gel column (10-35% EtOAc in Hexanes) to give 5-chloro-2-methylpyrido[3,4-b]pyrazin-3-yl methanesulfonate (1.68 g, 6.14 mmol, 64% yield) as a brown solid. MS (ESI, pos. ion) m/z: 274.0 (M+1); 1H NMR (400 MHz, CDCl3) δ ppm 8.59 (1H, d, J=5.7 Hz), 7.85 (1H, d, J=5.7 Hz), 3.83 (3H, s), 2.85 (3H, s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09394297B2
출처 데이터셋uspto-grants-2016_07
ORD IDord-f8ea379ae8ac40f2b9ce836df1c8fff0
출처 메모uspto-grants-2016_07