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HRID 32366作成日:2026年10月25日

Pyridine → 2-Chloro-N-{4-methyl-5-[2-(3-nitro-phenylamino)-pyrimidin-4-yl]-thiazol-2-yl}-acetamide

https://huagongshe.com/reaction/32366

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物AcetonitrileHCID 6342—
反応物Chloroacetyl chlorideHCID 6577—
反応物4-(2-Amino-4-methyl-5-thiazolyl)-N-(3-nitrophenyl)-2-pyrimidinamineHCID 447961—
溶媒DimethylformamideHCID 6228—
溶媒Trifluoroacetic acidHCID 6422—
生成物2-Chloro-N-{4-methyl-5-[2-(3-nitro-phenylamino)-pyrimidin-4-yl]-thiazol-2-yl}-acetamideHCID 10179394—

反応手順

A solution of [4-(2-amino-4-methyl-thiazol-5-yl)-pyrimidin-2-yl]-(3-nitro-phenyl)-amine (0.33 g, 1.0 mmol) in dry DMF (3 mL) was cooled on an ice-water bath. Chloroacetyl chloride (0.22 g, 2.0 mmol) and pyridine (80 μL) were added. After stirring at room temperature for 18 h, the product was isolated as a brown solid by preparative RP-HPLC (Vydac 218TP1022, 9 mL/min) using a gradient from 10-70% MeCN in 0.1% aq CF3COOH over 40 min. Anal. RP-HPLC: tR=20.62 min (Vydac 218TP54, 0-60% MeCN in 0.1% aq CF3COOH over 20 min, 1 mL/min, 25° C., purity >97%). 1H-NMR (DMSO-d6) δ: 2.45 (s, 3H, CH3), 4.12 (s, 2H, CH2), 7.03(d, 1H, J=5.2 Hz, pyrimidinyl-H), 7.42 (m, 1H, Ph-H), 7.63 (m, 1H, Ph-H), 8.01 (m, 1H, Ph-H), 8.41 (d, 1H, J=5.2 Hz, pyrimidinyl-H), 8.64 (s, 1H, Ph-H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07427627B2
出典データセットuspto-grants-2008_09
ORD IDord-0d39e5ff92d142fabe80ee9484ee6075
出典メモuspto-grants-2008_09