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HRID 1661004作成日:2026年10月25日

1,2-Dichloroethane → 5-[4-(5-Amino-3-tert-butyl-pyrazol-1-yl)-phenyl]-morpholin-4-yl-methanone

https://huagongshe.com/reaction/1661004

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DichloroethaneHCID 11—
反応物TetrahydrofuranHCID 8028—
反応物MorpholineHCID 8083—
反応物4-(5-Amino-3-tert-butyl-pyrazol-1-yl)-benzoic acidHCID 974688—
生成物5-[4-(5-Amino-3-tert-butyl-pyrazol-1-yl)-phenyl]-morpholin-4-yl-methanoneHCID 86625826—

反応手順

To a solution of 515 mg (1.98 mmol) 4-(5-amino-3-tert-butyl-pyrazol-1-yl)-benzoic acid and 259 μL (2.98 mMol) morpholine in 8 mL THF, 495 mg (2.58 mmol) of EDC are added at rt. The reaction is stirred at rt for 2 h. After completion, the resulting reaction mixture is concentrated and the residue is taken up in CH2Cl2, washed with brine (2×), dried and concentrated. The residual crude product is purified by flash chromatography (SiO2, CH2Cl2/MeOH; gradient 0-5% MeOH) to give the title compound as an off white powder. MS: [M+1]+=329.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08030311B2
出典データセットuspto-grants-2011_10
ORD IDord-8e7f78ea5e4b409cb5ef990d2f22fd7b
出典メモuspto-grants-2011_10