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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 44424생성일: 2026년 10월 26일

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

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Oxalyl chlorideHCID 65578—
반응물1-MethylxanthineHCID 80220—
반응물Aniline, p-isopropyl-N-methyl-HCID 138880—
용매ChloroformHCID 6212—
용매AcetonitrileHCID 6342—
생성물N-(4-isopropylphenyl)-N-methyl-2-(1-methyl-2,6-dioxo-1,2,3,6-tetrahydropurin-7-yl)acetamideHCID 5920510751%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541423B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-ea94e74472e04b1db751cf9295bd9520
출처 메모uspto-grants-2013_09