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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1185442생성일: 2026년 10월 26일

Triphenylphosphine → 4-((S)-2-{[4-((S)-1-Benzyloxycarbonyl-ethoxy)-7-methyl-quinoline-2-carbonyl]-amino}-3-tert-butoxycarbonyl-propionyl)-piperazine-1-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1185442

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물(R)-2-hydroxypropionic acid benzyl esterHCID 5324736—
반응물HCID 178473394HCID 178473394—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물4-((S)-2-{[4-((S)-1-Benzyloxycarbonyl-ethoxy)-7-methyl-quinoline-2-carbonyl]-amino}-3-tert-butoxycarbonyl-propionyl)-piperazine-1-carboxylic acid ethyl esterHCID 68597028—

반응 단계

To a solution of 1 g of 4-{(S)-3-tert-Butoxycarbonyl-2-[(4-hydroxy-7-methyl-quinoline-2-carbonyl)-amino]-propionyl}-piperazine-1-carboxylic acid ethyl ester and 350 mg of (R)-2-Hydroxy-propionic acid benzyl ester in 20 ml of THF, 764 mg of Triphenyl-phosphane and 507 mg of Diethyl azodicarboxylate was added and stirred for 2 h. Then, the reaction mixture was diluted with water and extracted with ethyl acetate. The organic phase was dried over MgSO4 and the solvents were removed under reduced pressure. The crude product was purified by chromatography on silica gel eluting with a gradient of n-heptane/ethyl acetate. The fractions containing the product were combined and the solvent evaporated under reduced pressure. Yield: 1.3 g.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08669266B2
출처 데이터셋uspto-grants-2014_03
ORD IDord-f34393a314d3414c9d1277363e0fbeee
출처 메모uspto-grants-2014_03