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HRID 60681作成日:2026年10月26日

Triphenylphosphine → HCID 117729796、化合物

https://huagongshe.com/reaction/60681

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物Diethyl azodicarboxylateHCID 5462977—
反応物3-Tetrahydropyranyloxy-1-propanolHCID 10855766—
反応物5-(5-amino-3-tert-butyl-1H-pyrazol-1-yl)-2-chlorophenolHCID 68952645—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 117729796HCID 11772979696%

反応条件

温度0 °C

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 in it is entirety; 500 mg, 1.88 mmol), and Ph3P (986 mg, 3.76 mmol) in dry THF (10 mL) was added 3-(tetrahydro-pyran-2-yloxy)-propan-1-ol (Can. J. Chem. Vol. 73, 1195, pp 1682, which is incorporated herein by reference in it is entirety; 452 mg, 2.82 mmol). The resulting mixture was cooled to 0° C. using an ice bath and diethylazodicarboxylate (0.69 mL, 3.76 mmol) was added to the chilled mixture which was allowed to warm up to RT. The volatiles were removed under reduced pressure. The residue was purified by FCC, using 0-50% EtOAc in cyclohexane, to give the title compound (739 mg, 96%). LCMS (Method 1): Rt 3.63 min, m/z 408 [MH+].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09440974B2
出典データセットuspto-grants-2016_09
ORD IDord-b2337666d511490898fa66a72f17d3a1
出典メモuspto-grants-2016_09