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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1296218생성일: 2026년 10월 26일

Ethyl Acetate → 2-{[(Benzyloxy)carbonyl]amino}-3-(3-{[(t-butoxycarbonyl)amino]methyl}-4-methoxyphenyl)-2-propenoic acid methyl ester

https://huagongshe.com/reaction/1296218

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물Tert-butyl (5-formyl-2-methoxybenzyl)carbamateHCID 22493931—
반응물[(Benzyloxy)carbonyl]amino-2-(dimethoxyphosphoryl)acetateHCID 131726531—
용매DichloromethaneHCID 6344—
생성물2-{[(Benzyloxy)carbonyl]amino}-3-(3-{[(t-butoxycarbonyl)amino]methyl}-4-methoxyphenyl)-2-propenoic acid methyl esterHCID 69485806—

반응 단계

2.65 g of t-butyl N-(5-formyl-2-methoxybenzyl)carbamate, 3.81 g of methyl 2-([(benzyloxy)carbonyl]amino-2-(dimethoxyphosphoryl)acetate and 1.75 g of 1,8-diazabicyclo[5,4,0]-7-undecene were dissolved in 50 ml of dichloromethane, followed by stirring for 15 hours at room temperature. 300 ml of ethyl acetate was added, and the organic layer was successively washed with 150 ml of water and 150 ml of brine, dried over magnesium sulfate and concentrated. The residue was purified by silica gel column chromatography, and 4.09 g of 2-{[(benzyloxy)carbonyl]amino}-3-(3-{[(t-butoxycarbonyl)amino]methyl}-4-methoxyphenyl)-2-propenoic acid methyl ester was obtained as a colorless solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07244861B2
출처 데이터셋uspto-grants-2007_07
ORD IDord-0477333a245b4dbf88326acc3540545d
출처 메모uspto-grants-2007_07