2-(4-Methoxypyrazol-1-yl)acetonitrile → Ethyl 1-(4-methoxy-1H-pyrazol-1-yl)cyclopropanecarbimidate
反応式
Cl[C:2]1[CH:3]=[N:4][N:5]([C:7]2([C:10](=[NH:14])[O:11][CH2:12][CH3:13])[CH2:9][CH2:8]2)[CH:6]=1.[CH3:15][O:16]C1C=NN(CC#N)C=1>>[CH3:15][O:16][C:2]1[CH:3]=[N:4][N:5]([C:7]2([C:10](=[NH:14])[O:11][CH2:12][CH3:13])[CH2:9][CH2:8]2)[CH:6]=1参加物
3
実験手順
The title compound was prepared by a method analogous to the one used for Intermediate 56, but using 2-(4-methoxy-1H-pyrazol-1-yl)acetonitrile as the starting material. 1H NMR (500 MHz, CDCl3) δ 1.37 (t, 3H), 1.63-1.72 (m, 4H), 3.76 (s, 3H), 4.16 (q, 2H), 7.17 (s, 1H), 7.35 (s, 1H).
出典と根拠
- ORDレコード
- ord-19bf543ae01d406194b4773585d10c1a
- 出典データセット
- uspto-grants-2016_03
- 特許番号
- US09296745B2
反応ノート
読み込み中…