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HRID 708604생성일: 2026년 10월 23일

Acetic Anhydride → N-(4-methyl-5-nitropyridin-2-yl)acetamide

https://huagongshe.com/ko/reaction/708604

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물2-Amino-4-methyl-5-nitropyridineHCID 243165—
생성물N-(4-methyl-5-nitropyridin-2-yl)acetamideHCID 13567013—

반응 단계

4-Methyl-5-nitro-pyridin-2-ylamine (1.0 g) was treated with acetic anhydride according to General Procedure Y to give N-(4-Methyl-5-nitro-pyridin-2-yl)-acetamide (1.1 g). LCMS (m/z): 196. N-(4-Methyl-5-nitro-pyridin-2-yl)-acetamide (0.5 g) was reduced under hydrogen atmosphere according to General Procedure Z to give N-(5-Amino-4-methyl-pyridin-2-yl)-acetamide (0.4 g), LCMS (m/z): 166. This was converted to 6-acetylamino-4-methyl-pyridine-3-sulfonyl chloride (0.35 g) according to General Procedure AA. LCMS (m/z): 249.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09175003B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-ca97001ecff64d6db670bfd2d546a10a
출처 메모uspto-grants-2015_11