Ammonia → HCID 44544870、化合物
反応式
[CH3:1][C:2]1[CH:14]=[C:5]2[N:6]=[CH:7][C:8]([C:11]([OH:13])=O)=[C:9]([CH3:10])[N:4]2[N:3]=1.O[N:16]=[C:17]([NH2:24])[C:18]1[CH:23]=[CH:22][CH:21]=[N:20][CH:19]=1.N>>[CH3:1][C:2]1[CH:14]=[C:5]2[N:6]=[CH:7][C:8]([C:11]3[O:13][N:24]=[C:17]([C:18]4[CH:19]=[N:20][CH:21]=[CH:22][CH:23]=4)[N:16]=3)=[C:9]([CH3:10])[N:4]2[N:3]=1参加物
4
実験手順
The title compound was prepared according Method C using 2,7-dimethylpyrazolo[1,5-a]pyrimidine-6-carboxylic acid (Maybridge) and N′-hydroxynicotinimidamide (Tyger). 1H NMR (300 MHz, DMSO-d6) δ2.52 (s, 3H), 3.27 (s, 3H), 6.77 (s, 1H), 7.67 (ddd, J=8.0, 4.9, 0.7 Hz, 1H), 8.48 (dt, J=8.6, 1.9 Hz, 1H), 8.84 (dd, J=4.7, 1.7 Hz, 1H), 9.06 (s, 1H), 9.30 (dd, J=2.2, 0.8 Hz, 1H), 9.30 (d, J=1.4 Hz, 1H) ppm; MS (DCI/NH3) m/z 293 (M+H)+.
出典と根拠
- ORDレコード
- ord-c9ea73302e0a469285156dfc7285dfd3
- 出典データセット