Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9209생성일: 2026년 10월 24일
Sodium Hydroxide → 7-(2-Methoxy-4,6-dimethylphenyl)-2-(methylsulfanyl)pyrazolo[1,5-a]pyridine-3-amine
https://huagongshe.com/ko/reaction/9209
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | tert-Butyl N-[7-(2-methoxy-4,6-dimethylphenyl)-2-(methylsulfanyl)pyrazolo[1,5-a]pyridin-3-yl]carbamate | HCID 21984503 | — |
| 용매 | Hydrogen chloride-ethyl acetate | HCID 21866389 | — |
| 생성물 | 7-(2-Methoxy-4,6-dimethylphenyl)-2-(methylsulfanyl)pyrazolo[1,5-a]pyridine-3-amine | HCID 21984486 | — |
반응 단계
tert-Butyl N-[7-(2-methoxy-4,6-dimethylphenyl)-2-(methylsulfanyl)pyrazolo[1,5-a]pyridin-3-yl]carbamate (50 mg) was dissolved in a 4 N hydrochloric acid/ethyl acetate solution (2 mL), and the mixture was stirred at room temperature for 1 hour. The reaction mixture was neutralized with 5 N aqueous sodium hydroxide and extracted with ethyl acetate, and the organic layer was concentrated to obtain 7-(2-methoxy-4,6-dimethylphenyl)-2-(methylsulfanyl)pyrazolo[1,5-a]pyridine-3-amine. This was dissolved in tetrahydrofuran (1 mL), and after adding propionaldehyde (0.078 mL) and 3 M aqueous sulfuric acid (0.363 mL), sodium borohydride (27 mg) was added in five portions at a time while vigorously stirring on ice, and stirring was continued for 30 minutes. After adding saturated aqueous sodium hydrogencarbonate to neutralize the reaction mixture, extraction was performed with ethyl acetate and the organic layer was concentrated. The residue was purified by silica gel column chromatography, and the title compound (20.6 mg) was obtained from the n-hexane:ethyl acetate (7:1) fraction 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-40db0070c5434809be40bc5733401f02 |
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| 출처 메모 | uspto-grants-2006_08 |
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