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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 132393생성일: 2026년 10월 25일

Sodium Bicarbonate → Methyl 3-{2-[(acetyloxy)methyl]-4-[(tert-butoxycarbonyl)amino]-3-methylphenyl}-2-{[(benzyloxy)carbonyl]amino}prop-2-enoate

https://huagongshe.com/reaction/132393

반응식

참여 물질

역할이름HCID투입량
반응물Sodium BicarbonateHCID 516892—
반응물Z-Dehydro-Ala-OMeHCID 3525700—
반응물3-(Tert-butoxycarbonylamino)-6-iodo-2-methylbenzyl acetateHCID 53414707—
촉매palladium(II) acetateHCID 167845—
촉매Tetrabutylammonium chloride hydrateHCID 16212273—
용매TetrahydrofuranHCID 8028—
생성물Methyl 3-{2-[(acetyloxy)methyl]-4-[(tert-butoxycarbonyl)amino]-3-methylphenyl}-2-{[(benzyloxy)carbonyl]amino}prop-2-enoateHCID 5341513869%

반응 단계

Palladium (II) acetate (105 mg, 0.43 mmol) was added to a mixture of acetic acid 3-tert-butoxycarbonylamino-6-iodo-2-methyl-benzyl ester (2.89 g, 7.1 mmol), Z-dehydroalanine methyl ester (2.20 g, 9.4 mmol), tetrabutylammonium chloride hydrate (2.70 g, 9.7 mmol), and sodium bicarbonate (1.80 g, 21.4 mmol) in THF (100 mL). Reaction was heated at reflux for 3.75 hours. Mixture was cooled to room temperature then filtered through a plug of silica gel eluting 70% ethyl acetate-hexanes (500 mL). Filtrate was concentrated in vacuo. Silica gel chromatography afforded the title compound as a yellow solid in 69% yield. 1H NMR (300 MHz, CDCl3): δ=7.79 (d, J=8.4, 1H), 7.42 (s, 1H), 7.27 (m, 6H), 6.30 (s, 1H), 5.11 (s, 2H), 5.02 (s, 2H), 3.81 (s, 3H), 2.21 (s, 3H), 2.02 (s, 3H), 1.51 (s, 9H). MS m/e (M−H)−=511.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07384931B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-352943eb1b0842e8995f4c02459a8d56
출처 메모uspto-grants-2008_06