(5-bromo-1-methyl-1H-pyrazol-4-yl)methanol → 5-bromo-1-methyl-1H-pyrazole-4-carbaldehyde
反応式
[Br:1][C:2]1[N:6]([CH3:7])[N:5]=[CH:4][C:3]=1[CH2:8][OH:9].C(C1C=CC(N2C(C=O)=CN=C2)=CC=1)C>>[Br:1][C:2]1[N:6]([CH3:7])[N:5]=[CH:4][C:3]=1[CH:8]=[O:9]参加物
3
実験手順
(5-Bromo-1-methyl-1H-pyrazol-4-yl)methanol (C23) was converted to the product using a procedure analogous to that described for the synthesis of 1-(4-ethylphenyl)-1H-imidazole-5-carbaldehyde (C19) in Example 5, step 3. In this case, no chromatography was carried out. Yield: 1.46 g, 7.72 mmol, 92%. LCMS m/z 191.2 (M+1). 1H NMR (400 MHz, CDCl3) δ 3.93 (s, 3H), 7.96 (s, 1H), 9.76 (s, 1H).
出典と根拠
- ORDレコード
- ord-63035b714f6c4ae0a51dcc15846a9d04
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08829010B2
反応ノート
読み込み中…