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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11366생성일: 2026년 10월 23일

Water → Tert-butyl 2-[(2,3-dimethyl-5-nitro-6-phenoxypyridin-4-yl)amino]ethylcarbamate

https://huagongshe.com/ko/reaction/11366

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물PhenolHCID 996—
반응물Sodium hydrideHCID 24758—
반응물Tert-butyl 2-[(2-chloro-5,6-dimethyl-3-nitropyridin-4-yl)amino]ethylcarbamateHCID 21973801—
용매DiglymeHCID 8150—
생성물Tert-butyl 2-[(2,3-dimethyl-5-nitro-6-phenoxypyridin-4-yl)amino]ethylcarbamateHCID 2197382359.1%

반응 조건

온도90 °C

반응 단계

Phenol (1.19 g, 12.6 mmol) was added in portions to a chilled (0° C.) suspension of sodium hydride (0.52 g of 60%, 13.1 mmol) in diglyme (4 mL). The reaction mixture was then stirred for 30 minutes. A warm solution of tert-butyl 2-[(2-chloro-5,6-dimethyl-3-nitropyridin-4-yl)amino]ethylcarbamate (3.0 g, 8.70 mmol) in diglyme (6 mL) was added and the reaction mixture was heated at 90° C. overnight. The reaction mixture was cooled and poured slowly into water (100 mL). The resulting tan solid was isolated by filtration, washed with water, dried and then recrystallized from isopropanol (25 mL) to provide 2.07 g of tert-butyl 2-[(2,3-dimethyl-5-nitro-6-phenoxypyridin-4-yl)amino]ethylcarbamate as white needles. The reaction was repeated using 66.5 g of starting material to provide 50.4 g of product as white needles, m.p. 158–160° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07098221B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-d6384d48d7884598a010228de80c34f6
출처 메모uspto-grants-2006_08