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

HRID 31363

反応式

HRID 31363 の反応式
[OH:1][C:2]1[C:10]([CH2:11][OH:12])=[C:9]2[C:5]([CH:6]=[N:7][N:8]2[CH2:13][C@@H:14]([NH:16][C:17](=[O:26])[O:18][CH2:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[CH3:15])=[CH:4][CH:3]=1>C(OCC)(=O)C>[CH:11]([C:10]1[C:2]([OH:1])=[CH:3][CH:4]=[C:5]2[C:9]=1[N:8]([CH2:13][C@@H:14]([NH:16][C:17](=[O:26])[O:18][CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)[CH3:15])[N:7]=[CH:6]2)=[O:12]

参加物

3

反応条件

温度
47.5 °C

実験手順

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.

後処理

  1. waitThen the reaction stood at room temperature one day
  2. filtrationThe mixture was filtered
  3. washthe black solids were rinsed with ethyl acetate
  4. customThe organic filtrate was evaporated to a tan foam
  5. customThe residue was purified by chromatography (silica gel, hexane/ethyl acetate 1:1)

出典と根拠

ORDレコード
ord-c9f6e9f88df6466cbf88d76d2fd5b741
出典データセット
uspto-grants-2008_09
特許番号
US07425572B2

関連ノート

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