Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9926생성일: 2026년 10월 25일
Oxazolo(4,5-b)pyridine → (S)-2-(tert-butoxycarbonyl)amino-1-(oxazolo[4,5-b]pyridin-2-yl)propan-1-ol
https://huagongshe.com/reaction/9926
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Oxazolo(4,5-b)pyridine | HCID 10103159 | — |
| 반응물 | tert-butyl N-((2S)-1-oxobutan-2-yl)carbamate | HCID 10241556 | — |
| 반응물 | HCID 178418918 | HCID 178418918 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (S)-2-(tert-butoxycarbonyl)amino-1-(oxazolo[4,5-b]pyridin-2-yl)propan-1-ol | HCID 69617110 | 43.5% |
반응 단계
In a clean roundbottom flask equipped with stir bar was placed oxazolo[4,5-b]pyridine (600 mg, 5 mmol) in 30 mL THF and the reaction mixture was cooled to 0° C. under N2 atmosphere. Isopropylmagnesium chloride (2M in THF, 2.5 ml, 5 mmol ) was added. After stirring for 1 h at 0° C., (S)-2-(tert-butoxycarbonyl)aminobutyraldehyde (573 mg, 3 mmol) in 20 ml THF was added. The ice bath was removed and the reaction mixture was allowed to warm to room temperature. After 2 h, the reaction mixture was quenched with saturated ammonium chloride solution and concentrated to dryness. The residue was extracted with EtOAc, then washed with brine, dried with anhyd. MgSO4, filtered and concentrated. The crude product was purified by chromatograph to yield 383 mg of the desired compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07091360B2 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-0f7f3745dfef454bbb9619689f26fde3 |
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| 출처 메모 | uspto-grants-2006_08 |
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