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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 78347생성일: 2026년 10월 23일

5-Amino-2-methylphenol → 4-(5-amino-2-methylphenoxy)-N-methylpyridine-2-carboxamide

https://huagongshe.com/ko/reaction/78347

반응식

참여 물질

역할이름HCID투입량
반응물5-Amino-2-methylphenolHCID 17818—
반응물4-Chloro-N-methylpicolinamideHCID 1476814—
생성물4-(5-amino-2-methylphenoxy)-N-methylpyridine-2-carboxamideHCID 23614556—

반응 단계

Entry 18: According to Method A2, Step 4, 5-amino-2-methylphenol was reacted with 4-chloro-N-methyl-2-pyridinecarboxamide, which had been synthesized according to Method A2, Step 3b, to give 3-(2-(N-methylcarbamoyl)-4-pyridyloxy)-4-methylaniline. 5-(Trifluoromethyl)-2-methoxyaniline was converted into 5-(trifluoromethyl)-2-methoxyphenyl isocyanate according to Method B1. 5-(Trifluoromethyl)-2-methoxyphenyl isocyanate was reacted with 3-(2-(N-methylcarbamoyl)-4-pyridyloxy)-4-methylaniline according to Method C1a to afford the urea.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841330B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-d83345b9e3ed4c89a71eb51d0f208525
출처 메모uspto-grants-2014_09