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HRID 31363作成日:2026年10月24日

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/ja/reaction/31363

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl {(1S)-2-[6-hydroxy-7-(hydroxymethyl)-1H-indazol-1-yl]-1-methylethyl}carbamateHCID 135427951—
溶媒Ethyl AcetateHCID 8857—
生成物Benzyl [(1S)-2-(7-formyl-6-hydroxy-1H-indazol-1-yl)-1-methylethyl]carbamateHCID 13638511435%

反応条件

温度47.5 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07425572B2
出典データセットuspto-grants-2008_09
ORD IDord-c9f6e9f88df6466cbf88d76d2fd5b741
出典メモuspto-grants-2008_09