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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11353생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/11353

반응식

참여 물질

역할이름HCID투입량
반응물tert-butyl N-(4-aminobutyl)carbamateHCID 4351—
반응물TriethylamineHCID 8471—
반응물2,4-Dichloro-5,6-dimethyl-3-nitropyridineHCID 12109123—
용매DimethylformamideHCID 6228—
생성물Tert-butyl 4-[(2-chloro-5,6-dimethyl-3-nitropyridin-4-yl)amino]butylcarbamateHCID 1210912448%

반응 단계

A solution of tert-butyl 4-aminobutylcarbamate (8.52 g, 45.24 mmol) in N,N-dimethylformamide was added to a solution of 2,4-dichloro-5,6-dimethyl-3-nitropyridine (10.00 g, 45.24 mmol) and triethylamine (12.6 mL, 90.5 mmol) in N,N-dimethylformamide (320 mL). The reaction mixture was stirred overnight and then concentrated under reduced pressure. The residue was partitioned between water and ethyl acetate. The layers were separated and the aqueous layer was extracted with ethyl acetate. The organics were combined, washed with brine and then concentrated under reduced pressure to provide a brown oily residue. This material was purified by flash chromatography (400 mL silica gel, eluting initially with 10% ethyl acetate in hexane and then increasing the gradient to 15% and then to 25%) to provide 8.1 g of tert-butyl 4-[(2-chloro-5,6-dimethyl-3-nitropyridin-4-yl)amino]butylcarbamate as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07098221B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-70c165635d014dcb99ca60dfce845323
출처 메모uspto-grants-2006_08