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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358020Generated: October 30, 2026

4-Methylmorpholine → HCID 13066725, compound

https://huagongshe.com/reaction/358020

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantSodium HydroxideHCID 14798—
ReactantIsobutyl chloroformateHCID 62365—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 12915689HCID 12915689—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13066725HCID 1306672546.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04464371
Source datasetuspto-grants-1984_08
ORD IDord-da64e97c408641469e1ab232d5e1eb0a
Source noteuspto-grants-1984_08