HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462869Generated: October 29, 2026
4-Methylmorpholine → HCID 53656047, compound
https://huagongshe.com/reaction/462869
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | N,N-Diethylethylenediamine | HCID 60993 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 13501986 | HCID 13501986 | — |
| Reactant | 2,5-Dioxopyrrolidin-1-yl N-[(benzyloxy)carbonyl]-O-tert-butyl-L-serinate | HCID 13819921 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 53656047 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04517119 |
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| Source dataset | uspto-grants-1985_05 |
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| ORD ID | ord-8c581baba7244a5392a89e2e9aa483c1 |
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| Source note | uspto-grants-1985_05 |
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