Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9196생성일: 2026년 10월 24일
Triethyl borate → 3-[(tert-Butoxycarbonyl)amino]-2-(methylsulfanyl)pyrazolo[1,5-a]pyridin-7-ylboric Acid
https://huagongshe.com/ko/reaction/9196
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethyl borate | HCID 9009 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | tert-Butyl N-[7-iodo-2-methylthiopyrazolo[1,5-a]pyridin-3-yl]carbamate | HCID 21984511 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 3-[(tert-Butoxycarbonyl)amino]-2-(methylsulfanyl)pyrazolo[1,5-a]pyridin-7-ylboric Acid | HCID 21984713 | — |
반응 단계
After dissolving tert-butyl N-(7-iodo-2-(methylsulfanyl)pyrazolo[1,5-a]pyridin-3-yl)carbamate (200 mg) in tetrahydrofuran (2 mL), the mixture was cooled to −78° C. and n-butyllithium (1.6 M; 0.66 mL) was added dropwise. The mixture was stirred for 1-hour at the same temperature, triethoxyborane (109 μL) was added and the temperature was increased to room temperature. Saturated aqueous ammonium chloride was added to the obtained reaction mixture, and extraction was performed with ethyl acetate. The obtained organic layer was washed with brine and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure to obtain the title compound (106 mg) as grayish white crystals.
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-f6b1679482d14db0b11eddb742d1b067 |
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| 출처 메모 | uspto-grants-2006_08 |
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