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HRID 56282作成日:2026年10月26日
Toluene → 3-(3-chloro-4-morpholinophenyl)-2-((3-chlorophenoxy)methyl)-6-methyl-pyrimidin-4(3H)-one
https://huagongshe.com/reaction/56282
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Toluene | HCID 1140 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | 2-(3-Chlorophenoxy)acetamide | HCID 2745969 | — |
| 反応物 | N-(3-chloro-4-morpholinophenyl)-3-oxobutanamide | HCID 90022603 | — |
| 触媒 | Titanium isopropoxide | HCID 11026 | — |
| 溶媒 | O-Xylene | HCID 7237 | — |
| 生成物 | 3-(3-chloro-4-morpholinophenyl)-2-((3-chlorophenoxy)methyl)-6-methyl-pyrimidin-4(3H)-one | HCID 90051700 | 64% |
反応手順
A mixture of N-(3-chloro-4-morpholinophenyl)-3-oxobutanamide (0.48 g, 1.62 mmol), 2-(3-chlorophenoxy)acetamide (0.60 g, 3.24 mmol) and titanium tetraisopropanolate (2.4 mL) in xylene (10 mL) was stirred at 165° C. for 24 h. The mixture was cooled to rt and 60 mL of toluene and 60 mL of saturated NH4Cl aqueous solution were added. The resulting mixture was stirred at rt overnight and filtered and the filtrate was extracted with DCM (20 mL×4). The combined organic layers were washed with brine (30 mL×2), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by a silica gel column chromatography (PE/EtOAc (V/V)=1:1) to give the title compound as a yellow solid (0.46 g, 64%). The compound was characterized by the following spectroscopic data:
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09434695B2 |
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| 出典データセット | uspto-grants-2016_09 |
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| ORD ID | ord-6dcbc20cf52e40a79ed93a3709ffb114 |
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| 出典メモ | uspto-grants-2016_09 |
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