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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 68299생성일: 2026년 10월 24일

N-Methylbenzeneethanamine → 2-(N-methylphenethylamino)-6-phenylpyrimidine-4-carboxamide

https://huagongshe.com/ko/reaction/68299

반응식

참여 물질

역할이름HCID투입량
반응물N-MethylbenzeneethanamineHCID 11503—
반응물DiisopropylethylamineHCID 81531—
반응물HCID 58872694HCID 58872694—
용매1,4-DioxaneHCID 31275—
생성물2-(N-methylphenethylamino)-6-phenylpyrimidine-4-carboxamideHCID 1560354651.7%

반응 조건

온도85 °C

반응 단계

2-Methanesulfonyl-6-phenylpyrimidine-4-carboxamide (70 mg, 0.25 mmol), 1,4-dioxane (4 mL), DIPEA (0.3 mL, 2.0 mmol) and N-methylphenethylamine (82 mg, 0.6 mmol) were added to a 8 mL vial. The vial was sealed and heated at 85° C. for two days. The reaction mixture was allowed to cool to room temperature, and the solvent then removed by centrifugal evaporation. The residue was purified by preparative HPLC to afford 43 mg of 2-(N-methylphenethylamino)-6-phenylpyrimidine-4-carboxamide. 1H NMR (CDCl3, 300 MHz) δ 8.14 (m, 2H), 7.74 (s, 1H), 7.67 (br s, 1H), 7.47 (m, 3H), 7.25 (m, 5H), 5.79 (br s, 1H), 3.95 (t, J=6.9 Hz, 2H), 3.21 (s, 3H), 2.97 (t, J=6.9 Hz, 2H). HPLC ret. time 3.25 min, 10-100% CH3CN, 5 min run. ESI-MS m/z 333.3 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822451B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-0539cb802972482dbf0f1709587fadb3
출처 메모uspto-grants-2014_09