化工社化工社 化学情報印刷レポート · 研究参考用
1,2-Dichloroethane → 5-[4-(5-Amino-3-tert-butyl-pyrazol-1-yl)-phenyl]-morpholin-4-yl-methanone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1,2-Dichloroethane | HCID 11 | — |
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | Morpholine | HCID 8083 | — |
| 反応物 | 4-(5-Amino-3-tert-butyl-pyrazol-1-yl)-benzoic acid | HCID 974688 | — |
| 生成物 | 5-[4-(5-Amino-3-tert-butyl-pyrazol-1-yl)-phenyl]-morpholin-4-yl-methanone | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08030311B2 |
| 出典データセット | uspto-grants-2011_10 |
| ORD ID | ord-8e7f78ea5e4b409cb5ef990d2f22fd7b |
| 出典メモ | uspto-grants-2011_10 |