돌아가기
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

반응식

참여 물질

역할이름HCID투입량
반응물Oxazolo(4,5-b)pyridineHCID 10103159—
반응물tert-butyl N-((2S)-1-oxobutan-2-yl)carbamateHCID 10241556—
반응물HCID 178418918HCID 178418918—
용매TetrahydrofuranHCID 8028—
생성물(S)-2-(tert-butoxycarbonyl)amino-1-(oxazolo[4,5-b]pyridin-2-yl)propan-1-olHCID 6961711043.5%

반응 조건

온도0 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091360B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-0f7f3745dfef454bbb9619689f26fde3
출처 메모uspto-grants-2006_08