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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 458699생성일: 2026년 10월 24일

Benzenemethanamine, 3,4-dimethyl- → n-(3,4-Dimethylbenzyl)-6-hydroxy-1-methyl-2,5-dioxo-1,2,3,5-tetrahydroimidazo[1,2-a]pyrimidine-7-carboxamide

https://huagongshe.com/ko/reaction/458699

반응식

참여 물질

역할이름HCID투입량
반응물Benzenemethanamine, 3,4-dimethyl-HCID 66888—
반응물Ethyl 6-hydroxy-1-methyl-2,5-dioxo-1,2,3,5-tetrahydroimidazo[1,2-a]pyrimidine-7-carboxylateHCID 54725632—
생성물n-(3,4-Dimethylbenzyl)-6-hydroxy-1-methyl-2,5-dioxo-1,2,3,5-tetrahydroimidazo[1,2-a]pyrimidine-7-carboxamideHCID 5470430258%

반응 단계

Reaction of intermediate 13, ethyl 6-hydroxy-1-methyl-2,5-dioxo-1,2,3,5-tetrahydroimidazo[1,2-a]pyrimidine-7-carboxylate (0.070 g, 0.28 mmol) with 3,4-dimethylbenzylamine (0.15 g, 1.12 mmol) as described in the preparation of example 1 gave 0.042 g (58% yield) of the title amide as a white solid. 1HNMR 400 MHz (DMSO-d6) δ (ppm): 2.18 (3H, s, CH3), 2.20 (3H, s, CH3), 3.14 (3H, s, NCH3), 4.42 (2H, d, J=6.3 Hz, NCH2), 4.47 (2H, s, CH2), 7.0–7.1 (3H, m, aromatics), 9.40 (1H, broad t, NH), 12.35 (1H, s, OH). MS (ESI+) m/z 343 [M+H+].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07192948B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-c6017042c8b2404ab0c98e074b43aa1d
출처 메모uspto-grants-2007_03