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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 31362생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/31362

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물Sodium HydroxideHCID 14798—
반응물Benzyl (S)-2-(6-hydroxy-1H-indazol-1-yl)-1-methylethylcarbamateHCID 135487328—
용매TetrahydrofuranHCID 8028—
생성물Benzyl {(1S)-2-[6-hydroxy-7-(hydroxymethyl)-1H-indazol-1-yl]-1-methylethyl}carbamateHCID 135427951—

반응 단계

A solution of benzyl [(1S)-2-(6-hydroxy-1H-indazol-1-yl)-1-methylethyl]carbamate (30.83 g, 0.0949 mol) in THF (400 ml) was treated with aqueous concentrated formaldehyde (37%, 12 M. 0.285 mol, 24 mL) and cooled in an ice bath. To the mixture was slowly added aqueous 1 N sodium hydroxide (0.02 mol, 20 mL) and the reaction was allowed to warm to room temperature while stirring overnight. The reaction was quenched with aqueous saturated sodium bicarbonate (250 mL) and then neutralized to pH 7 with aqueous 2 N hydrochloric acid. The mixture was extracted with ethyl acetate (200 mL×3), the combined organic layers were dried over magnesium sulfate and filtered and evaporated to give crude tan solid, 28.38 g, which was a mixture of desired product and dimerized byproduct by LC/MS 356 m/z and 663 m/z. This residue was purified by chromatography (silica gel, hexane/ethyl acetate 1:1) to give the title compound, (18.44 g, 56%) as a yellow foamy solid, which was not pure by LS/MS 354 m/z with minor 663 m/z.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425572B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-bfb01c5aa2d84f0398523e4456f98058
출처 메모uspto-grants-2008_09