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HRID 1959394Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1959394

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium BicarbonateHCID 516892—
Edukt3-amino-6-(4-ethylsulfonylpiperazin-1-yl)-N-phenacyl-pyrazine-2-carboxamideHCID 66745451—
LösungsmittelSulfuric AcidHCID 1118—
Produkt5-(4-(Ethylsulfonyl)piperazin-1-yl)-3-(5-phenyloxazol-2-yl)pyrazin-2-amineHCID 667444336%

Reaktionsschritte

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

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08410112B2
Quelldatensatzuspto-grants-2013_04
ORD IDord-c523891bce054fcdab0d1a0484ae5983
Quellennotizuspto-grants-2013_04