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HRID 637009作成日:2026年10月26日

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

https://huagongshe.com/reaction/637009

反応式

関与物質

役割名称HCID仕込み量
反応物4-MethylmorpholineHCID 7972—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物Fmoc-L-Asp(OtBu)-OHHCID 2724635—
反応物PyBOPHCID 2724699—
反応物L-Tryptophan benzyl esterHCID 7016092—
溶媒DichloromethaneHCID 6344—
生成物Fmoc-Asp(Ot-Bu)-Trp-OBzlHCID 13172240677.3%

反応条件

温度0 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06194195B1
出典データセットuspto-grants-2001_02
ORD IDord-a1b71068972c44c1aac4fac5267b2b84
出典メモuspto-grants-2001_02