HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358020Generated: October 30, 2026
4-Methylmorpholine → HCID 13066725, compound
https://huagongshe.com/reaction/358020
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | HCID 12915689 | HCID 12915689 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13066725 | HCID 13066725 | 46.3% |
Reaction Steps
3.1 g of N--methylmorpholine is added to 180 ml of dry tetrahydrofuran solution of 12.5 g of (2R,4R)--3--(S--benzoyl--3--mercaptopropionyl) --2--(2--hydroxyphenyl)--4--thiazolidine--carboxylic acid. To the reaction mixture, 4.1 g of isobutyl chlorocarbonate is added dropwise while stirring under ice-cooling and further stirred for 30 minutes at the same temperature. To this suspension, 120 ml of methanol solution containing 6.3 g of hydroxylamine hydrochloride and 3.6 g of sodium hydroxide is added dropwise, and stirred for 2 hours by gradually restoring the room temperature. The solvent is removed in vacuo, and N hydrochloric acid is added to the resulting residue. Separated oil is extracted with ethyl acetate, and the organic layer is washed with saturated sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent is removed in vacuo and the resulting oily residue is purified by silica gel coulumn chromatography to give 6.0 g of the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04464371 |
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| Source dataset | uspto-grants-1984_08 |
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| ORD ID | ord-da64e97c408641469e1ab232d5e1eb0a |
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| Source note | uspto-grants-1984_08 |
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