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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 730408생성일: 2026년 10월 24일

4-Methylmorpholine → tert-butyl N-{4'-[3-(N'-butyrylhydrazino)-2-ethoxy-3-oxopropyl]biphenyl-3-ylmethyl}-N-methylcarbamate

https://huagongshe.com/ko/reaction/730408

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물Ethyl AcetateHCID 8857—
반응물DiisopropylcarbodiimideHCID 12734—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물ButyrohydrazideHCID 77079—
반응물3-{3'-[(Tert-butoxycarbonylmethylamino)methyl]biphenyl-4-yl}-2-ethoxypropionic acidHCID 68852083—
용매TetrahydrofuranHCID 8028—
생성물tert-butyl N-{4'-[3-(N'-butyrylhydrazino)-2-ethoxy-3-oxopropyl]biphenyl-3-ylmethyl}-N-methylcarbamateHCID 68852131100%

반응 조건

온도-5 °C

반응 단계

0.15 ml (1.33 mmol) of N-methylmorpholine is added to a solution of 0.5 g (1.2 mmol) of 3-{3′-[(tert-butoxycarbonylmethylamino)methyl]biphenyl-4-yl}-2-ethoxypropionic acid, 0.14 g (1.3 mmol) of butyric hydrazide and 0.33 g (2.4 mmol) of 1-hydroxybenzotriazole in 10 ml of tetrahydrofuran cooled to −5° C. After stirring for 5 minutes, 0.2 ml (1.3 mmol) of diisopropylcarbodiimide is added. The reaction medium is stirred at 0° C. for 1 hour and then at room temperature for 2 hours, diluted with ethyl acetate, washed with saturated aqueous caesium hydrogen carbonate solution, extracted with ethyl acetate, dried over magnesium sulfate, filtered and concentrated. The residue obtained is chromatographed on a column of silica eluted with a 1/1 heptane/ethyl acetate mixture. 0.6 g of tert-butyl N-{4′-[3-(N′-butyrylhydrazino)-2-ethoxy-3-oxopropyl]biphenyl-3-ylmethyl}-N-methylcarbamate is obtained in a yield of 100%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07582663B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-232fb9bc676e4d25827e2f4eb22ebbce
출처 메모uspto-grants-2009_09