Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15014생성일: 2026년 10월 24일
p-Toluenesulfonic acid → 2-{6-[2-(2-Chlorophenyl)-5-(4-propoxyphenyl)-pyrrol-1ylmethyl]-2-nitro-pyridin-3-yloxy}-ethanol
https://huagongshe.com/ko/reaction/15014
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | p-Toluenesulfonic acid | HCID 6101 | — |
| 반응물 | Chloroform | HCID 6212 | — |
| 반응물 | 1-(2-Chlorophenyl)-4-(4-propoxyphenyl)-butane-1,4-dione | HCID 16090339 | — |
| 반응물 | Acetic acid 2-(6-aminomethyl-2-nitropyridin-3-yloxy)-ethyl ester | HCID 59341182 | — |
| 용매 | 2-Methylphenethyl alcohol | HCID 88267 | — |
| 생성물 | 2-{6-[2-(2-Chlorophenyl)-5-(4-propoxyphenyl)-pyrrol-1ylmethyl]-2-nitro-pyridin-3-yloxy}-ethanol | HCID 59341200 | 32.6% |
반응 단계
To a solution of 0.2 gm of acetic acid 2-(6-aminomethyl-2-nitropyridin-3-yloxy)-ethyl ester (0.8 mmol) in 3 mL of 5:1 toluene-ethanol was added 0.20 gm of 1-(2-chlorophenyl)-4-(4-propoxyphenyl)-butane-1,4-dione and 10 mg of p-TsOH. The reaction mixture stirred at 100° C. for 72 h. The reaction mixture was poured into 200 mL of CHCl3 and washed twice with water (100 mL), saturated brine, dried (Na2SO4), and the solvents removed under reduced pressure. The residue was purified by column chromatography using 4% methanol-chloroform as an eluent to give 100 mg (25% yield) of an oil. This was used without further purification or characterization.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07732457B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-54e07e9af4464f6988cfab1ed5303406 |
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| 출처 메모 | uspto-grants-2010_06 |
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