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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1815003생성일: 2026년 10월 25일

tert-butyl N-(4-aminobutyl)carbamate → Tert-butyl 4-(2-chloro-5,6-dimethyl-3-nitropyridin-4-yl)butylcarbamate

https://huagongshe.com/reaction/1815003

반응식

참여 물질

역할이름HCID투입량
반응물tert-butyl N-(4-aminobutyl)carbamateHCID 4351—
반응물DimethylformamideHCID 6228—
반응물TriethylamineHCID 8471—
반응물2,4-Dichloro-5,6-dimethyl-3-nitropyridineHCID 12109123—
용매Ethyl AcetateHCID 8857—
생성물Tert-butyl 4-(2-chloro-5,6-dimethyl-3-nitropyridin-4-yl)butylcarbamateHCID 2197383079.8%

반응 단계

Tert-butyl 4-aminobutylcarbamate (60 g, 339 mmol) was slowly added to a mixture of 2,4-dichloro-5,6-dimethyl-3-nitropyridine (50 g, 226 mmol), anhydrous N,N-dimethylformamide (500 mL) and triethylamine (50 mL, 339 mmol). The reaction mixture was allowed to stir overnight and then it was concentrated under reduced pressure to provide an oil. The oil was dissolved in ethyl acetate and then washed with water. The organic layer was dried over magnesium sulfate and then concentrated under reduced pressure to provide a dark oil. This material was purified by column chromatography (silica gel eluting with 40/60 ethyl acetate/hexanes) to provide 64.5 g of tert-butyl 4-(2-chloro-5,6-dimethyl-3-nitropyridin-4-yl)butylcarbamate as a bright orange oil which solidified on standing.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06878719B2
출처 데이터셋uspto-grants-2005_04
ORD IDord-a4e528e845d94c189584dfcd74255a8e
출처 메모uspto-grants-2005_04