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HRID 416283作成日:2026年10月26日

3-Dimethylamino-1-(3-pyridyl)-2-propen-1-one → 4-(4-(Pyridin-3-yl)pyrimidin-2-ylamino)benzoic acid

https://huagongshe.com/reaction/416283

反応式

関与物質

役割名称HCID仕込み量
反応物3-Dimethylamino-1-(3-pyridyl)-2-propen-1-oneHCID 5369165—
反応物(E)-3-(Dimethylamino)-1-(pyrazin-2-YL)prop-2-EN-1-oneHCID 5825354—
反応物4-[(4-Pyrazin-2-yl-pyrimidin-2-ylamino)-methyl]-benzoic acidHCID 66622167—
反応物HCID 178512548HCID 178512548—
生成物4-(4-(Pyridin-3-yl)pyrimidin-2-ylamino)benzoic acidHCID 14346970—

反応手順

Title compound was prepared according to the procedure described for the synthesis of compound 25a (scheme 6, step 3) replacing the guanindine 24 by 4-guanidinobenzoic acid (344) (Zlatoidsky P., Maliar T. Eur. J. Med. Chem Chim. Ther.; 1996, 31, 895-900) and (E)-3-(dimethylamino)-1-(pyrazin-2-yl)-prop-2-en-1-one (23a) by (E)-3-(dimethylamino)-1-(pyridin-3-yl)prop-2-en-1-one (345) (Zimmermann J., Buchdunger E., et al. Bioorg. Med. Chem. Lett., 1996, 6, 1221-1226). Yield of the product 28%. MS (m/z): 292.29 (calc) 293.1 (MH+) (found).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08088805B2
出典データセットuspto-grants-2012_01
ORD IDord-aee82466963b472296b51e3e048c19ac
出典メモuspto-grants-2012_01