反応式
Cl[C:2]1[C:7]([CH:8]=[O:9])=[C:6]([Cl:10])[N:5]=[C:4]([S:11][CH3:12])[N:3]=1.[CH3:13][CH:14]([NH2:17])[CH2:15][CH3:16]>>[CH:14]([NH:17][C:2]1[C:7]([CH:8]=[O:9])=[C:6]([Cl:10])[N:5]=[C:4]([S:11][CH3:12])[N:3]=1)([CH2:15][CH3:16])[CH3:13]参加物
3
実験手順
Prepared as described above in Example 2 starting from 4,6-dichloro-2-methylsulfanyl-pyrimidine-5-carbaldehyde and 2-butylamine to give the title compound 4-sec-butylamino-6-chloro-2-methylsulfanyl-pyrimidine-5-carbaldehyde. 1H-NMR: δ 0.87 (m, 3H), 1.18 (m, 3H), 1.20 (m, 2H), 2.51 (s, 3H), 4.24 (m, 1H), 9.12 (br s, 1H), 10.18 (s, 1H). LC MS (m/e)=260 (MH+).
後処理
- customPrepared
出典と根拠
- ORDレコード
- ord-0bde9e7647ac499891cb149e3e5e4199
- 出典データセット
- uspto-grants-2011_11
- 特許番号
- US08058282B2
関連ノート
読み込み中…