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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 453376생성일: 2026년 10월 24일

Diisopropylamine → 2-methyl-5-nitro-N-(pyrimidin-5-yl)benzamide

https://huagongshe.com/ko/reaction/453376

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylamineHCID 7912—
반응물Pyrimidin-5-amineHCID 344373—
반응물2-Methyl-5-nitrobenzoic acidHCID 519683—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
용매DimethylformamideHCID 6228—
생성물2-methyl-5-nitro-N-(pyrimidin-5-yl)benzamideHCID 24823255—

반응 단계

In a 2L round bottom flask with mechanical stirring was charged with 2-methyl-5-nitrobenzoic acid (20 g), HATU (38 g) and diisopropylamine (32 mL) in DMF (90 mL). This mixture was stirred for 30 min then pyrimidin-5-amine was added and the reaction was stirred for 18 hr. The LCMS showed complete conversion. DMF was removed under vacuum as much as possible then water was added and a solid precipitated out (use mechanical stirring). The tan solid was filtered and rinsed with water, then taken up in EtOAc, washed with brine, dried over MgSO4, filtered and concentrated down. The crude was taken up in EtOAc and the product 45 precipitated out. This was filtered and the filtrate was concentrated down and taken up in EtOAc/Hex. After standing overnight, more solids were filtered and were combined with the first crop. 2-methyl-5-nitro-N-(pyrimidin-5-yl)benzamide 45 was obtained as a light yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08492404B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-8412d5d5f20e47908513066372e957b3
출처 메모uspto-grants-2013_07