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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637009Generated: October 25, 2026

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

https://huagongshe.com/reaction/637009

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantFmoc-L-Asp(OtBu)-OHHCID 2724635—
ReactantPyBOPHCID 2724699—
ReactantL-Tryptophan benzyl esterHCID 7016092—
SolventDichloromethaneHCID 6344—
ProductFmoc-Asp(Ot-Bu)-Trp-OBzlHCID 13172240677.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06194195B1
Source datasetuspto-grants-2001_02
ORD IDord-a1b71068972c44c1aac4fac5267b2b84
Source noteuspto-grants-2001_02