Bromine → 4-Bromomethyl-5-propyl-6-chloro-pyrimidine
反応式
[Br:1]Br.[CH2:3]([C:6]1[C:7]([Cl:13])=[N:8][CH:9]=[N:10][C:11]=1[CH3:12])[CH2:4][CH3:5]>CC(O)=O>[CH2:3]([C:6]1[C:7]([Cl:13])=[N:8][CH:9]=[N:10][C:11]=1[CH2:12][Br:1])[CH2:4][CH3:5]参加物
4
反応条件
- 温度
- 85 °C
実験手順
Br2 (1.28 g, 8 mmol) is added dropwise to a stirred solution 101 in HOAc (20 ml) heated at 85° C. After addition, the mixture is stirred at 85° C. for 1 hour. The solvent is removed in vacuo and EtOAc (25 ml) and NaHCO3 (25 ml) are added to the residue. The layers are separated and the organic layer is washed with Na2S2O3 solution (sat. 15 ml) followed by brine (20 ml). The organic phase is dried (Na2SO4) and evaporated. The resulting yellow oil is purified by flash column (6:1 EtOAc, hexane) to afford the product (102) as a light yellow solid.
後処理
- additionAfter addition
- customThe solvent is removed in vacuo and EtOAc (25 ml) and NaHCO3 (25 ml)
- additionare added to the residue
- customThe layers are separated
- washthe organic layer is washed with Na2S2O3 solution (sat. 15 ml)
- dry with materialThe organic phase is dried (Na2SO4)
- customevaporated
- customThe resulting yellow oil is purified by flash column (6:1 EtOAc, hexane)
出典と根拠
- ORDレコード
- ord-67ae873481174f1e89bb9b2cdb9646f3
- 出典データセット
- uspto-grants-2007_09
- 特許番号
- US07271170B2
反応ノート
読み込み中…