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HRID 272515作成日:2026年10月27日

5-Morpholinopyridin-2-amine → 8-cyclopentyl-6-ethoxymethyl-2-(5-morpholin-4-yl-pyridin-2-ylamino)-8H-pyrido[2,3-d]pyrimidin-7-one

https://huagongshe.com/reaction/272515

反応式

関与物質

役割名称HCID仕込み量
反応物5-Morpholinopyridin-2-amineHCID 11367346—
反応物8-cyclopentyl-6-ethoxymethyl-2-methanesulfinyl-8H-pyrido[2,3-d]pyrimidin-7-oneHCID 11772012—
溶媒TolueneHCID 1140—
生成物8-cyclopentyl-6-ethoxymethyl-2-(5-morpholin-4-yl-pyridin-2-ylamino)-8H-pyrido[2,3-d]pyrimidin-7-oneHCID 1021699317.6%

反応手順

8-Cyclopentyl-6-ethoxymethyl-2-methanesulfinyl-8H-pyrido[2,3-d]pyrimidin-7-one (0.60 g, 1.79 mmol) and 5-morpholin-4-yl-pyridin-2-ylamine (0.442 g, 2.47 mmol) were heated to reflux in toluene (6 mL) for 16 hours. The reaction mixture was cooled to room temperature and the precipitate that formed was filtered off and washed with toluene (2×4 mL) to give 8-cyclopentyl-6-ethoxymethyl-2-(5-morpholin-4-yl-pyridin-2-ylamino)-8H-pyrido[2,3-d]pyrimidin-7-one (0.142 g, 17.6%). MS (APCl); M++1: Calc'd, 451.3. Found 451.3. Anal. Calc'd for C25H32N6O2: C, 63.98; H, 6.71; N, 18.65. Found; C, 64.03; H, 6.66; N, 18.49.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07456168B2
出典データセットuspto-grants-2008_11
ORD IDord-51ccefb81b8443b2acb698f1d470d581
出典メモuspto-grants-2008_11