Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 56282생성일: 2026년 10월 24일
Toluene → 3-(3-chloro-4-morpholinophenyl)-2-((3-chlorophenoxy)methyl)-6-methyl-pyrimidin-4(3H)-one
https://huagongshe.com/ko/reaction/56282
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Toluene | HCID 1140 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | 2-(3-Chlorophenoxy)acetamide | HCID 2745969 | — |
| 반응물 | N-(3-chloro-4-morpholinophenyl)-3-oxobutanamide | HCID 90022603 | — |
| 촉매 | Titanium isopropoxide | HCID 11026 | — |
| 용매 | O-Xylene | HCID 7237 | — |
| 생성물 | 3-(3-chloro-4-morpholinophenyl)-2-((3-chlorophenoxy)methyl)-6-methyl-pyrimidin-4(3H)-one | HCID 90051700 | 64% |
반응 단계
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:
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09434695B2 |
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| 출처 데이터셋 | uspto-grants-2016_09 |
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| ORD ID | ord-6dcbc20cf52e40a79ed93a3709ffb114 |
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| 출처 메모 | uspto-grants-2016_09 |
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