HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359769Generated: October 29, 2026
4-Methylmorpholine → HCID 10408263, compound
https://huagongshe.com/reaction/359769
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | HCID 10093047 | HCID 10093047 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 10408263 | HCID 10408263 | 54.1% |
Reaction Steps
1,5 ml of N-methylmorpholine was added, whilst ice-cooling, to a solution of 1.74 g of (2S, 3S)-3-(2- amino-5-phenoxyphenyl)thio-2-hydroxy-3-(4-methoxyphenyl)propionic acid [prepared as described in step (b) above] and 1,5 g of diphenylphosphorylaZide dissolved in 19 ml of dimethylformamide, and the mixture was stirred at room temperature for 16 hours. At the end of this time, ethyl acetate and water were added to the reaction mixture, and the resulting mixture was shaken to mix it thoroughly The ethyl acetate layer was then separated and dried over anhydrous magnesium sulfate, and the solvent was removed by evaporation under reduced pressure. The crystalline residue was collected by filtration using diethyl ether and diisopropyl ether to afford 0.90 g of the title compound melting at 181-183° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05002942 |
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| Source dataset | uspto-grants-1991_03 |
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| ORD ID | ord-09ad636c9c214e5f9cf548f3682c1c72 |
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| Source note | uspto-grants-1991_03 |
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