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HRID 44424作成日:2026年10月26日

Dimethylformamide → N-(4-isopropylphenyl)-N-methyl-2-(1-methyl-2,6-dioxo-1,2,3,6-tetrahydropurin-7-yl)acetamide

https://huagongshe.com/reaction/44424

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Oxalyl chlorideHCID 65578—
反応物1-MethylxanthineHCID 80220—
反応物Aniline, p-isopropyl-N-methyl-HCID 138880—
溶媒ChloroformHCID 6212—
溶媒AcetonitrileHCID 6342—
生成物N-(4-isopropylphenyl)-N-methyl-2-(1-methyl-2,6-dioxo-1,2,3,6-tetrahydropurin-7-yl)acetamideHCID 5920510751%

反応手順

To a solution of acid 120 (0.25 g, 1.11 mmol) in CHCl3 (20 mL) and CH3CN (20 mL) at 0° C. was added oxalyl chloride (0.84 g, 6.69 mmol) and a catalytic amount of DMF. The resulting solution was stirred for 2 h at rt and concentrated in vacuo. The residue was re-dissolved in CHCl3 and the resulting solution cooled to 0° C. To this mixture was added N-methyl-4-isopropyl aniline (0.29 g, 2 mmol) and the reaction was stirred overnight warming to rt. The reaction was then diluted with CHCl3 (30 mL) and washed with 1 N HCl (50 mL). The combined organic layers were washed with water (75 mL), dried over Na2SO4 and concentrated in vacuo and the product was purified by chromatography on silica gel eluting with EtOAc/hexanes and EtOAc/MeOH to yield 392 (0.2 g, 51%) as a light brown solid. mp: 271-273° C. MS (APCI): m/z 356.2 [H+H]+ Anal. Calcd. For C18H21N5O3. 0.35 H2O: C, 59.77; H, 6.05; N, 19.36. Found C, 59.77; H, 6.07; N, 19.29.

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-ea94e74472e04b1db751cf9295bd9520
出典メモuspto-grants-2013_09