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HRID 3450作成日:2026年10月23日

Dimethylformamide dimethyl acetal → N'-[6-(2,6-dichlorophenyl)-2-{3-(diethylamino)propylamino}-pyrido[2,3-d]pyrimidin-7-yl]-N,N-dimethylformamidine

https://huagongshe.com/ja/reaction/3450

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethylformamide dimethyl acetalHCID 78373—
反応物6-(2,6-dichlorophenyl)-2-N-[3-(diethylamino)propyl]pyrido[2,3-d]pyrimidine-2,7-diamineHCID 5328114—
溶媒DimethylformamideHCID 6228—
生成物N'-[6-(2,6-dichlorophenyl)-2-{3-(diethylamino)propylamino}-pyrido[2,3-d]pyrimidin-7-yl]-N,N-dimethylformamidineHCID 532817468%

反応手順

To a suspension of 210 mg (1 mmol) of 7-amino-6-(2,6-dichlorophenyl)-2-[3-(diethylamino) propylamino]-pyrido[2,3-d]pyrimidine from Example 20 in 0.8 mL of DMF was added 0.8 mL of DMF dimethyl acetal. The mixture was stirred at room temperature for 5.5 hours, then concentrated in vacuo. The residual oil was distributed between dichloromethane and water. The organic phase was dried over magnesium sulfate, then concentrated to a glass that was crystallized from acetonitrile to give 160 mg (68%) of N'-[6-(2,6-dichlorophenyl)-2-{3-(diethylamino) propylamino}-pyrido[2,3-d]pyrimidin-7-yl]-N, N-dimethylformamidine, mp 100°-104° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05733913
出典データセットuspto-grants-1998_03
ORD IDord-3b18944e08c244489c0c882a36845a09
出典メモuspto-grants-1998_03