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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 647393생성일: 2026년 10월 25일

4-Methylmorpholine → Boc-Leu-Gln-Arg(Tos)-Leu-OH

https://huagongshe.com/reaction/647393

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물AminoethylpiperazineHCID 8795—
반응물Boc-Leu-OSuHCID 11023929—
반응물HCID 178427537HCID 178427537—
촉매PalladiumHCID 23938—
용매MethanolHCID 887—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물Boc-Leu-Gln-Arg(Tos)-Leu-OHHCID 17842753383%

반응 단계

In 235 ml of N-methylpyrrolidone are dissolved 16.9 g (24 millimoles) of Z-Gln-Arg(Tos)-Leu-OH obtained according to the process of Example 1 and 8.7 g (26.4 millimoles) of Boc-Leu-OSu, and 2.64 ml of N-methylmorpholine is added to the solution. Then, 3 g of 10% Pd-C is added to the mixture, and the mixture is stirred for 5 hours in a current of H2. Then, N-(2-aminoethyl) piperazine is added to the mixture, the mixture is stirred for 1 hour and 100 ml of methanol is added to the mixture. The 10% Pd-C is recoved by filtration, and the mixture is concentrated under reduced pressure to distill N-methylpyrrolidone. The residue is added to a liquid mixture of 100 ml of ethyl acetate and 200 ml of a dilute aqueous solution of citric acid. The mixture is sufficiently stirred, and the ethyl acetate layer is recovered, washed with water, dried and concentrated under reduced pressure. Ether is added to the concentrate and the precipitate is recovered by filtration to obtain 15.6 g of intended Boc-Leu-Gln-Arg(Tos)-Leu-OH (the yield being 83.2%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04407745
출처 데이터셋uspto-grants-1983_10
ORD IDord-7d4697dbb33f44bb9df5956ccf7a0bd3
출처 메모uspto-grants-1983_10