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HRID 3451作成日:2026年10月24日

Dimethylformamide dimethyl acetal → N'-[7-(3-tert-butylureido)-6-(2,6-dichlorophenyl)-pyrido[2,3-d]pyrimidin-2-yl]-N,N-dimethylformamidine

https://huagongshe.com/ja/reaction/3451

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1-(2-Amino-6-(2,6-dichlorophenyl)pyrido[2,3-d]pyrimidin-7-yl)-3-(tert-butyl)ureaHCID 5328112—
生成物N'-[7-(3-tert-butylureido)-6-(2,6-dichlorophenyl)-pyrido[2,3-d]pyrimidin-2-yl]-N,N-dimethylformamidineHCID 54357764—

反応手順

1-[2-Amino-6-(2,6-dichlorophenyl)-pyrido[2,3-d]pyrimidin-7-yl]-3-tert-butylurea from Example 3 was reacted with DMF dimethyl acetal for 13.5 hours as described in Example 78. Workup as described above, followed by purification on flash silica gel chromatography eluting sequentially with 100:0, 3:1, 1:1, and 0:100 dichloromethane:ethyl acetate gave a solid that was triturated in 2-propanol to afford the title compound N'-[7-(3-tert-butylureido)-6-(2,6-dichlorophenyl)-pyrido[2,3-d]pyrimidin-2-yl]-N,N-dimethylformamidine, mp 190°-193° 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-72ff6e6fed6a469e82049eb403a60197
出典メモuspto-grants-1998_03