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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1959394생성일: 2026년 10월 27일

Sodium Bicarbonate → 5-(4-(Ethylsulfonyl)piperazin-1-yl)-3-(5-phenyloxazol-2-yl)pyrazin-2-amine

https://huagongshe.com/reaction/1959394

반응식

참여 물질

역할이름HCID투입량
반응물Sodium BicarbonateHCID 516892—
반응물3-amino-6-(4-ethylsulfonylpiperazin-1-yl)-N-phenacyl-pyrazine-2-carboxamideHCID 66745451—
용매Sulfuric AcidHCID 1118—
생성물5-(4-(Ethylsulfonyl)piperazin-1-yl)-3-(5-phenyloxazol-2-yl)pyrazin-2-amineHCID 667444336%

반응 단계

3-amino-6-(4-ethylsulfonylpiperazin-1-yl)-N-phenacyl-pyrazine-2-carboxamide (80 mg, 0.1850 mmol) in H2SO4 (1.5 mL) was stirred at ambient temperature for 16 hours. The reaction was neutralised by addition of NaHCO3 solution and then extracted with EtOAc (3×), combined organics dried (MgSO4) and concentrated in vacuo. The resultant residue was purified by reverse phase preparative HPLC [Waters Sunfire C18, 10 uM, 100A column, gradient 10%-95% B (solvent A: 0.05% TFA in water, solvent B: CH3CN) over 16 minutes at 25 mL/min]. The fractions were collected and freeze-dried to give the title compound as an orange solid (4.5 mg, 6% Yield). 1H NMR (DMSO) d 1.25 (3H, t), 3.11 (2H, q), 3.35 masked signal, 3.54 (4H, m), 7.00 (2H, br s), 7.42 (1H, m), 7.53 (2H, m), 7.84 (2H, m), 7.99 (1H, s), 8.14 (1H, s) ppm; MS (ES+) 415.0

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08410112B2
출처 데이터셋uspto-grants-2013_04
ORD IDord-c523891bce054fcdab0d1a0484ae5983
출처 메모uspto-grants-2013_04