돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 637009생성일: 2026년 10월 25일

4-Methylmorpholine → Fmoc-Asp(Ot-Bu)-Trp-OBzl

https://huagongshe.com/reaction/637009

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물Fmoc-L-Asp(OtBu)-OHHCID 2724635—
반응물PyBOPHCID 2724699—
반응물L-Tryptophan benzyl esterHCID 7016092—
용매DichloromethaneHCID 6344—
생성물Fmoc-Asp(Ot-Bu)-Trp-OBzlHCID 13172240677.3%

반응 조건

온도0 °C

반응 단계

41 mg of Fmoc-Asp(Ot-Bu)-OH was dissolved in 2 ml of methylene chloride, and the solution was cooled to 0° C. 78 mg of PyBOP, 20 mg of HOBt and 22 μl of NMM were added thereto in order and stirring was effected for 5 minutes, at 0° C. 2 ml of the methylene chloride solution containing 34 mg of H-Trp-OBzl (NO2) as obtained above was cooled to 0° C. and then added to the resulting reaction solution. Stirring was effected at 4° C. for 4 hours and at room temperature for 1 hour, the solvent was evaporated under reduced pressure, and the residue was purified with a silica gel column (manufactured by Merck Co., Kieselgel 60, 50 g, elution with chloroform:methanol=25:1), to obtain 53 mg of Fmoc-Asp(Ot-Bu)-Trp-OBzl (NO2). The obtained product was dissolved in 100 μl of DMF, 25 μl of piperidine was added. The mixture was then allowed to stand at room temperature for 10 minutes, and purified with a silica gel column (manufactured by Merck Co., Kieselgel 60, 50 g, elution with hexane:ethyl acetate=2:1), to obtain 1 mg of H-Asp(Ot-Bu)-Trp-OBzl (NO2).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06194195B1
출처 데이터셋uspto-grants-2001_02
ORD IDord-a1b71068972c44c1aac4fac5267b2b84
출처 메모uspto-grants-2001_02