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HRID 1453作成日:2026年10月23日

Dimethylamine → 6-dimethylamino-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinone

https://huagongshe.com/ja/reaction/1453

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylamineHCID 674—
反応物6-chloro-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinoneHCID 19690700—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物6-dimethylamino-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinoneHCID 19690695—

反応手順

To an ice cooled solution of 1.5 g (3.8 mmol) 6-chloro-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinone in 4 mL of tetrahydrofuran, was added 22 mL (99 mmol) of 4.5M dimethylamine in ether portionwise (2-4 mL) over a period of 7 days. The reaction mixture was allowed to warm and stir at room temperature after each addition. The progress of the reaction was followed by gas chromatography and proceeded to 80% completion. The solvent was removed in vacuo and the residue was taken up in ether and washed twice with water. The organic layer was dried over MgSO4 and concentrated to yield 1.15 g crude solid product. Flash column chromatography on silica gel (gradient elution 25-30% ethyl acetate-hexane) afforded pure 6-dimethylamino-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinone (compound 23), as a white solid. 1H-NMR (CDCl3) δ 2.2(3H,s); 2.35(1H,t); 3.5(6H,s); 4.6(2H,d); 7.65(3H,m); 7.75(2H,m).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05726124
出典データセットuspto-grants-1998_03
ORD IDord-c771bb9653f84a339085fb2d456f388e
出典メモuspto-grants-1998_03