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HRID 711145作成日:2026年10月26日

Triphenylphosphine → 5-tert-Butyl-2-[4-chloro-3-(2-morpholin-4-yl-ethoxy)-phenyl]-2H-pyrazol-3-ylamine

https://huagongshe.com/reaction/711145

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物1-MorpholinoethanolHCID 3029376—
反応物Diethyl azodicarboxylateHCID 5462977—
反応物5-(5-amino-3-tert-butyl-1H-pyrazol-1-yl)-2-chlorophenolHCID 68952645—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物5-tert-Butyl-2-[4-chloro-3-(2-morpholin-4-yl-ethoxy)-phenyl]-2H-pyrazol-3-ylamineHCID 11772970680%

反応手順

To a stirred solution of 5-(5-amino-3-tert-butyl-pyrazol-1-yl)-2-chloro-phenol (WO2007/091152, which is incorporated herein by reference; 200 mg, 0.75 mmol), 2-N morpholino ethanol (137 μL, 1.13 mmol) and Ph3P (394 mg, 1.50 mmol) in THF (7.5 mL) at 0° C. was added DEAD (236 μL, 1.50 mmol). After 1 h, the reaction mixture was diluted with water and extracted with DCM. The combined organics were dried and concentrated in vacuo. The residue was purified by FCC, using 0-5% [2M NH3 in MeOH] in DCM, to give the title compound (228 mg, 80%). LCMS (Method 3): Rt 2.28 min, m/z 379 [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-ce89b2b57f7b48d5837cb9af3fc1799e
出典メモuspto-grants-2015_11