돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 31363생성일: 2026년 10월 24일

Benzyl {(1S)-2-[6-hydroxy-7-(hydroxymethyl)-1H-indazol-1-yl]-1-methylethyl}carbamate → Benzyl [(1S)-2-(7-formyl-6-hydroxy-1H-indazol-1-yl)-1-methylethyl]carbamate

https://huagongshe.com/ko/reaction/31363

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl {(1S)-2-[6-hydroxy-7-(hydroxymethyl)-1H-indazol-1-yl]-1-methylethyl}carbamateHCID 135427951—
용매Ethyl AcetateHCID 8857—
생성물Benzyl [(1S)-2-(7-formyl-6-hydroxy-1H-indazol-1-yl)-1-methylethyl]carbamateHCID 13638511435%

반응 조건

온도47.5 °C

반응 단계

A solution of the compound from Step A (18.44 g, 0.0519 mol) in ethyl acetate (180 mL) was treated with mangenese dioxide (fine powder, 18 g) and stirred at 45-50° C. for two days. Then the reaction stood at room temperature one day. The mixture was filtered and the black solids were rinsed with ethyl acetate. The organic filtrate was evaporated to a tan foam. The residue was purified by chromatography (silica gel, hexane/ethyl acetate 1:1) to give the title compound, (6.32 g, 35%) as a pale yellow fluffy solid, which was pure by LS/MS 354 m/z.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425572B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-c9f6e9f88df6466cbf88d76d2fd5b741
출처 메모uspto-grants-2008_09