反応式
[NH2:1][C:2]1[CH:3]=[N:4][CH:5]=[N:6][CH:7]=1.C(#N)C.[Cl:11][CH2:12][C:13](Cl)=[O:14]>ClCCCl>[Cl:11][CH2:12][C:13]([NH:1][C:2]1[CH:3]=[N:4][CH:5]=[N:6][CH:7]=1)=[O:14]参加物
5
反応条件
- 温度
- 80 °C
実験手順
5-Aminopyrimidine (450 mg) was suspended in DCE (2 mL) and acetonitrile (2 mL) in a microwave vial. Chloroacetyl chloride (0.377 mL) was added with stirring. The vial was sealed and the reaction mixture was heated in the microwave at 80° C. for 5 minutes. The solid was filtered off, washed with acetonitrile (2×5 mL), DCE (2×5 mL) and pentane (2 ×30 mL) and then partioned between saturated sodium bicarbonate and DCE (50 mL/50 mL) ensuring the aqueous layer was still basic. The organic layer was separated and the aqueous layer was extracted with DCE (2×75 mL). The combined organic layer was dried over magnesium sulfate and evaporated to give the sub-titled compound (200 mg) as a yellow solid.
後処理
- customThe vial was sealed
- filtrationThe solid was filtered off
- washwashed with acetonitrile (2×5 mL), DCE (2×5 mL) and pentane (2 ×30 mL)
- customThe organic layer was separated
- extractionthe aqueous layer was extracted with DCE (2×75 mL)
- dry with materialThe combined organic layer was dried over magnesium sulfate
- customevaporated
出典と根拠
- ORDレコード
- ord-4a31dca5b97042f5afd384119e29a258
- 出典データセット
- uspto-grants-2012_12
- 特許番号
- US08329729B2
関連ノート
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