反応式
[N:1]([CH2:4][C:5]1[CH:9]=[CH:8][N:7]([C:10]2[CH:15]=[CH:14][C:13]([I:16])=[CH:12][CH:11]=2)[N:6]=1)=[N+]=[N-]>CO.[Ni]>[I:16][C:13]1[CH:12]=[CH:11][C:10]([N:7]2[CH:8]=[CH:9][C:5]([CH2:4][NH2:1])=[N:6]2)=[CH:15][CH:14]=1参加物
4
実験手順
A mixture of 3-(azidomethyl)-1-(4-iodophenyl)-1H-pyrazole (100 mg, 0.31 mmol) and Ra—Ni (50% aq. slurry, 150 mg) in MeOH (8 mL) was hydrogenated under balloon H2 for 3 hrs. It was filtered through celite. The filtrate was concentrated in vacuo to give (1-(4-iodophenyl)-1H-pyrazol-3-yl)methanamine (78 mg).
後処理
- filtrationIt was filtered through celite
- concentrationThe filtrate was concentrated in vacuo
出典と根拠
- ORDレコード
- ord-a56343b3dbb74dd782d128e53a759453
- 出典データセット
- uspto-grants-2010_04
- 特許番号
- US07696352B2
関連ノート
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