Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9201생성일: 2026년 10월 23일
Propanal → N-[7-(2,4-Dichlorophenyl)-2-ethylpyrazolo[1,5-a]pyridin-3-yl]-N-(2-methoxyethyl)-N-propylamine
https://huagongshe.com/ko/reaction/9201
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Propanal | HCID 527 | — |
| 반응물 | Sulfuric Acid | HCID 1118 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 반응물 | N-[7-(2,4-Dichlorophenyl)-2-ethylpyrazolo[1,5-a]pyridin-3-yl]-N-(2-methoxyethyl)amine | HCID 21984623 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-[7-(2,4-Dichlorophenyl)-2-ethylpyrazolo[1,5-a]pyridin-3-yl]-N-(2-methoxyethyl)-N-propylamine | HCID 21984679 | — |
반응 단계
N-[7-(2,4-Dichlorophenyl)-2-ethylpyrazolo[1,5-a]pyridin-3-yl]-N-(2-methoxyethyl)amine (14 mg) was dissolved in tetrahydrofuran (1 mL), and after adding propionaldehyde (0.016 mL) and 3 M aqueous sulfuric acid (0.77 mL), sodium borohydride (5.8 mg) was added in five portions while vigorously stirring on ice, and stirring was continued for 30 minutes. Water was added to the reaction mixture, extraction was performed with diethyl ether and the extract was washed with saturated aqueous sodium hydrogencarbonate and brine. After drying over anhydrous magnesium sulfate and filtration, the solvent was concentrated under reduced pressure and the residue was purified by preparative TLC [n-hexane:ethyl acetate (5:1), Rf=0.5] to obtain the title compound (9.5 mg) as a light yellow oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07091215B2 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-5add00d2fc5045eab00f8af0fde67517 |
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| 출처 메모 | uspto-grants-2006_08 |
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