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HRID 220572作成日:2026年10月27日

Triethylamine → {4-[4-(1-Ethyl-1H-pyrazol-4-ylmethyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyrazinyl-3'-yl]-phenyl}-methanol hydrochloride

https://huagongshe.com/reaction/220572

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Ammonium ChlorideHCID 25517—
反応物1-Ethyl-1H-pyrazole-4-carboxaldehydeHCID 2758900—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物[4-(3,4,5,6-tetrahydro-2H-[1,2']bipyrazinyl-3'-yl)-phenyl]-methanol dihydrochlorideHCID 68595263—
溶媒Acetic AcidHCID 176—
溶媒MethanolHCID 887—
溶媒1,1-DichloroethaneHCID 6365—
溶媒Sodium BicarbonateHCID 516892—
生成物{4-[4-(1-Ethyl-1H-pyrazol-4-ylmethyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyrazinyl-3'-yl]-phenyl}-methanol hydrochlorideHCID 6859550683.1%

反応手順

Combine [4-(3,4,5,6-tetrahydro-2H-[1,2′]bipyrazinyl-3′-yl)-phenyl]-methanol dihydrochloride (0.177 g, 0.516 mmol), 1-ethyl-1H-pyrazole-4-carbaldehyde (0.064 g, 0.516 mmol) and triethylamine (0.144 mL, 1.03 mmol) in dichloroethane (4 mL). Add glacial acetic acid (42 mL) followed by sodium triacetoxyborohydride (0.153 g, 0.722 mmol). Stir at room temperature for 20 hr. Dilute with saturated aq. sodium bicarbonate then extract three times using DCM. Dry (sodium sulfate), filter, concentrate and purify (silica gel chromatography, eluting with 4.5:95.5 methanol (with 2 M ammonia):DCM), to give a white solid. Dissolve the solid in methanol and add ammonium chloride (1 equivalent) then sonicate the mixture for 10 min. Evaporate the solution to give the title compound as a white solid (0.178 g, 83%). MS (ES): m/z=379

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08202873B2
出典データセットuspto-grants-2012_06
ORD IDord-01fb991012494ad28fc6df9defbb02b9
出典メモuspto-grants-2012_06