돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 32344생성일: 2026년 10월 24일

Pyridine → 2-Anilino-4-[1-isopropyl-2-(methoxyiminomethyl)imidazol-5-yl]pyrimidine

https://huagongshe.com/ko/reaction/32344

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물O-Methylhydroxylamine hydrochlorideHCID 521874—
반응물2-Anilino4-(2-formyl-1-isopropylimidazol-5-yl)pyrimidineHCID 11638102—
용매EthanolHCID 702—
생성물2-Anilino-4-[1-isopropyl-2-(methoxyiminomethyl)imidazol-5-yl]pyrimidineHCID 8676072691%

반응 단계

Methoxylamine hydrochloride (340 mg, 4.07 mmol) and pyridine (322 mg, 4.07 mmol) was added to a solution of 2-anilino-4-(2-formyl-1-isopropylimidazol-5-yl)pyrimidine (Example 10; 250 mg, 0.814 mmol) in EtOH (10 ml) and the mixture was stirred at ambient temperature for 18 hours. The volatiles were removed by evaporation and the residue triturated with water. The solid product was collected by filtration and dried at 50° C. under vacuum to give the title compound (248 mg, 91%) as a white crystalline solid. NMR (CDCl3): 1.54 (d, 6H), 4.07 (s, 3H), 5.65-5.80 (sept, 1H), 6.95 (d, 1H), 7.15 (m, 2H), 7.34 (t, 2H), 7.50 (s 1H), 7.57 (d, 2H), 8.28 (s, 1H), 8.41 (d, 1 H); m/z 337.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07427626B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-1abed8ef4cef491fbb24b1d7b8cc1856
출처 메모uspto-grants-2008_09