Morpholine → 2-Chloro-4-morpholinofuro[3,2-d]pyrimidine
反応式
[Cl:1][C:2]1[N:3]=[C:4](Cl)[C:5]2[O:10][CH:9]=[CH:8][C:6]=2[N:7]=1.[NH:12]1[CH2:17][CH2:16][O:15][CH2:14][CH2:13]1>CO>[Cl:1][C:2]1[N:3]=[C:4]([N:12]2[CH2:17][CH2:16][O:15][CH2:14][CH2:13]2)[C:5]2[O:10][CH:9]=[CH:8][C:6]=2[N:7]=1参加物
4
実験手順
2,4-Dichlorofuro[3,2-d]pyrimidine 37 (23 mg, 1.0 eq) was suspended in methanol (1.7 ml) and treated with morpholine (0.09 ml, 4.0 eq). Reaction mixture was stirred at room temperature for 2 h, before being quenched with saturated aq. NaHCO3. Mixture was extracted with dichloromethane. The combined organic layers were dried (Na2SO4) and concentrated to yield 2-chloro-4-morpholinofuro[3,2-d]pyrimidine 38 (14 mg, 48%) which was used in the next reaction without further purification.
後処理
- customReaction mixture
- custombefore being quenched with saturated aq. NaHCO3
- extractionMixture was extracted with dichloromethane
- dry with materialThe combined organic layers were dried (Na2SO4)
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-af65e09f594f4e208c058c8d92086afc
- 出典データセット
- uspto-grants-2013_02
- 特許番号
- US08383620B2
反応ノート
読み込み中…