反応式
[NH:1]([C:8]1[N:13]=[C:12]([CH3:14])[CH:11]=[C:10]([C:15]#[C:16][CH3:17])[N:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[S:18](=[O:22])(=[O:21])([OH:20])[OH:19]>C(O)C>[S:18]([OH:22])([OH:21])(=[O:20])=[O:19].[NH:1]([C:8]1[N:13]=[C:12]([CH3:14])[CH:11]=[C:10]([C:15]#[C:16][CH3:17])[N:9]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1参加物
4
実験手順
2-Anilino-4-methyl-6-(1-propynyl)pyrimidine (2.2 g) was dissolved in 100 ml of ethanol, and 2 ml of concentrated sulfuric acid was added thereto and stirred for 1 hour at room temperature. The crystals deposited were filtered, and dried to afford 2.4 g of 2-anilino-4-methyl-6-(1-propynyl)pyrimidine sulfate (yield 75%). Melting point: 192°-195° C.
後処理
- filtrationThe crystals deposited were filtered
- customdried
出典と根拠
- ORDレコード
- ord-779349712d9b4d689c7b0472cb9cb28a
- 出典データセット
- uspto-grants-1991_01
- 特許番号
- US04988704
関連ノート
読み込み中…