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HRID 44428作成日:2026年10月25日

Acefylline → HCID 45254481、化合物

https://huagongshe.com/reaction/44428

反応式

関与物質

役割名称HCID仕込み量
反応物AcefyllineHCID 69550—
反応物2-(4-Aminophenyl)propan-2-olHCID 9543261—
反応物Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
溶媒N,N-dimethylformamide; methylsulfinylmethaneHCID 3013483—
生成物HCID 45254481HCID 45254481—

反応手順

To a 0° C. solution of acid 101 (0.32 g, 1.34 mmol) in DMF/DMSO (1:1, 20 mL) was added HATU (0.0.76 g, 2.01 mmol). The reaction was then stirred an additional 15 min at room temperature. The solution was cooled to 0° C. and amine 135 (0.30 g, 2.01 mmol) was added. The reaction was then stirred at rt overnight. The DMF was concentrated in vacuo and water was added to the reaction. The aqueous layer was extracted with EtOAc The ethyl acetate layer was then washed again with water and the organic layer was concentrated in vacuo. The product was purified by flash chromatography on silica gel eluting with EtOAc/hexanes and EtOAc/MeOH to yield 402 as a pure light brown semi solid (0.086 g, 17.5%). MS (APCI): m/z 372.2 [M−H]+ Anal. Calcd. For C18H21N5O4. 0.35 EtOAc: C, 57.93; H, 5.96; N, 17.41. Found C, 58.36; H, 6.14; N, 16.96.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541423B2
出典データセットuspto-grants-2013_09
ORD IDord-baba062cb47f4c34aaf02c30011c1cd1
出典メモuspto-grants-2013_09