Morpholine → 4-Isopropylamino-2-morpholino-thieno[3,4-d]pyrimidine
反応式
Cl[C:2]1[N:3]=[C:4]([NH:11][CH:12]([CH3:14])[CH3:13])[C:5]2[C:6](=[CH:8][S:9][CH:10]=2)[N:7]=1.[NH:15]1[CH2:20][CH2:19][O:18][CH2:17][CH2:16]1>O>[CH:12]([NH:11][C:4]1[C:5]2[C:6](=[CH:8][S:9][CH:10]=2)[N:7]=[C:2]([N:15]2[CH2:20][CH2:19][O:18][CH2:17][CH2:16]2)[N:3]=1)([CH3:14])[CH3:13]参加物
4
実験手順
6 g (0.26 moles) of 2-chloro-4-isopropylamino-thieno[3,4-d]pyrimidine and 25 mls. of morpholine are mixed and then heated under reflux for 4 hours. The mixture is cooled and poured into water with vigorous agitation; a brown solid appears, which is separated by filtration, washed with water and put to dry. The product is converted into the maleate, which is recrystallized from acetone. The free base is obtained again by treatment with alkali and is this way one obtains 3.4 g of pure product. M.P. 202°C. with decomposition.
後処理
- temperatureheated
- temperatureunder reflux for 4 hours
- temperatureThe mixture is cooled
- customa brown solid appears, which is separated by filtration
- washwashed with water
- customto dry
- customis recrystallized from acetone
- customThe free base is obtained again by treatment with alkali and
出典と根拠
- ORDレコード
- ord-685980e4ef7b491d939a9d7691cb4c6f
- 出典データセット
- uspto-grants-1976_01
- 特許番号
- US03931204
反応ノート
読み込み中…