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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464552Generated: October 29, 2026

4-Methylmorpholine → FMOC-Asp(OBzl)-Glu(O-tBu)-Tyr(Bzl)-OBzl

https://huagongshe.com/reaction/464552

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantPiperidineHCID 8082—
ReactantIsobutyl chloroformateHCID 62365—
ReactantFMOC-Glu(OtBu)-Tyr(Bzl)-OBzlHCID 13534309—
Reactant(2S)-4-(Benzyloxy)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-oxobutanoic acidHCID 13966931—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductFMOC-Asp(OBzl)-Glu(O-tBu)-Tyr(Bzl)-OBzlHCID 1353431172%

Reaction Conditions

Temperature-15 °C

Reaction Steps

FMOC-Asp(OBzl) (4.45 g; 10 mmol) was dissolved in ethyl acetate (30 ml) and cooled down to -15° C. Isobutylchloroformate (1.5 ml; 11 mmol) was added to the solution, followed by N-methylmorpholine (1.2 ml; 11 mmol). FMOC-Glu(O-t-Bu)-Tyr(Bzl)-OBzl (29) (6 g; 7.8 mmol) was treated with 10% piperidine in dimethylformamide (100 ml) for 1 h. The solvent was removed under reduced pressure and the residue was dissolved in dimethylformamide (30 ml) and added to the first solution at -15° C. The reaction mixture was stirred overnight at ambient temperature. Solids were removed by filtration and under reduced pressure. The residue was dissolved in ethylacetate (150 ml) and the insoluble material was removed by filtration. The organic solution washed with 0.05N hydrochloric acid (3×40 ml), water (40 ml) and dried over anhydrous sodium sulfate. The drying agent was removed by filtration and the filtrate evaporated under reduced pressure. The residue was crystallized from ethylacetate/petroleum ether to give 5.5 g (72 percent) of 30, m.p. 96°-99° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04547489
Source datasetuspto-grants-1985_10
ORD IDord-f585bddfd0df458a98c3ea66c1e91b91
Source noteuspto-grants-1985_10