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HRID 711160作成日:2026年10月27日

Triphenylphosphine → 5-tert-Butyl-2-{4-chloro-3-[2-(tetrahydro-pyran-2-yloxy)-ethoxy]-phenyl}-2H-pyrazol-3-ylamine

https://huagongshe.com/reaction/711160

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物2-(Oxan-2-yloxy)ethan-1-olHCID 4166833—
反応物Diethyl azodicarboxylateHCID 5462977—
反応物5-(5-amino-3-tert-butyl-1H-pyrazol-1-yl)-2-chlorophenolHCID 68952645—
触媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物5-tert-Butyl-2-{4-chloro-3-[2-(tetrahydro-pyran-2-yloxy)-ethoxy]-phenyl}-2H-pyrazol-3-ylamineHCID 11772962989%

反応手順

To a solution of 5-(5-Amino-3-tert-butyl-pyrazol-1-yl)-2-chloro-phenol (WO2011/154734A1, which is incorporated herein by reference, 340 mg, 1.28 mmol), 2-(tetrahydro-pyran-2-yloxy)-ethanol (0.26 mL, 1.92 mmol) and Ph3P (671 mg, 2.56 mmol) in dry THF (10 mL) was added diethylazodicarboxylate (0.41 mL, 2.56 mmol) and the mixture stirred for 10 min. Water (4 drops) was added and the mixture concentrated in vacuo. The residue was purified by FCC, using 0-50% EtOAc in cyclohexane, to give the title compound (450 mg, 89%). LCMS (Method 3): Rt 3.73 min, m/z 394 [MH+].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09181242B2
出典データセットuspto-grants-2015_11
ORD IDord-e456be74a24947f1bd15604d214bf89f
出典メモuspto-grants-2015_11