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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 453353생성일: 2026년 10월 24일

Triethylamine → N-(2-aminopyrimidin-5-yl)-2-methyl-5-nitrobenzamide

https://huagongshe.com/ko/reaction/453353

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Pyrimidine-2,5-diamineHCID 229075—
반응물2-Methyl-5-nitrobenzoic acidHCID 519683—
용매Thionyl ChlorideHCID 24386—
생성물N-(2-aminopyrimidin-5-yl)-2-methyl-5-nitrobenzamideHCID 16118604—

반응 단계

2-methyl-5-nitrobenzoic acid (659 mg, 3.64 mmol) was heated to reflux in SOCl2 (6 mL) for 1 h. After cooling to room temperature and concentrating to dryness, the crude acid chloride was taken up in CH2Cl2 (25 mL). Pyrimidine-2,5-diamine 7 (400 mg, 3.64 mmol) was added to the solution and the mixture was allowed to stir at rt over night. The mixture became a thick white suspension. NEt3 (700 L, 4.73 mmol) was added. After 2 h, a thick white suspension remained. The mixture was filtered through a Buchner funnel and washed with copious amounts of CH2Cl2 to remove NEt3HCl salt, affording N-(2-aminopyrimidin-5-yl)-2-methyl-5-nitrobenzamide 8 as an off-white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08492404B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-ed21a3494afc44138dba256196849147
출처 메모uspto-grants-2013_07