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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462869Generated: October 29, 2026

4-Methylmorpholine → HCID 53656047, compound

https://huagongshe.com/reaction/462869

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantN,N-DiethylethylenediamineHCID 60993—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 13501986HCID 13501986—
Reactant2,5-Dioxopyrrolidin-1-yl N-[(benzyloxy)carbonyl]-O-tert-butyl-L-serinateHCID 13819921—
CatalystPalladiumHCID 23938—
SolventDimethylformamideHCID 6228—
ProductHCID 53656047HCID 53656047—

Reaction Steps

Z-Asp(OtBu)-Ala-OBzl (43.6 g, 90 mmol) was dissolved in 1 liter DMF and hydrogenated in the presence of Tos-OH.H2O (17.1 g, 90 mmol) and 10% Pd-C. After the hydrogenation was completed the catalyst was filtered off. The filtrate was cooled to 0°, neutralized with N-methylmorpholine (9.9 ml, 90 mmol) and added to Z-Ser(tBu)-OSu. Another portion of N-methylmorpholine (9.9 ml, 90 mmol) was added and the reaction mixture was stirred at 0° for 1 h and at 25° for 18 h. 2-Diethylamino-ethylamine (2.83 ml, 20 mmol) was added to the reaction mixture and stirring was continued for 4 h. The solution was evaporated in vacuo, the residue dissolved in 0.5N NaOH (0.5 l) and extracted with ether (3×0.2 l). To the alkaline phase 0.4 l ethyl acetate was added and acidified with 5% KHSO4 /10% K2SO4 -solution. The acidic layer was again extracted with ethyl acetate (2×0.3 l). The combined organic layers were washed with 5% KHSO4 /10% K2SO4 -sol. (1×0.3 l) and saturated NaCl-sol., dried over Na2SO4, filtered and evaporated in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04517119
Source datasetuspto-grants-1985_05
ORD IDord-8c581baba7244a5392a89e2e9aa483c1
Source noteuspto-grants-1985_05