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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545116Generated: October 25, 2026

Water → (2S)-N-{[4-(3,4-dichlorobenzyl)morpholin-2-yl]methyl}-[4-(hydroxymethyl)thiazol-2-ylthio]acetamide

https://huagongshe.com/reaction/545116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantLithium ChlorideHCID 433294—
ReactantSodium borohydrideHCID 4311764—
Reactant(2S)-N-{[4-(3,4-dichlorobenzyl)morpholin-2-yl]methyl}-[4-(ethoxycarbonyl)thiazol-2-ylthio]acetamideHCID 67170480—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product(2S)-N-{[4-(3,4-dichlorobenzyl)morpholin-2-yl]methyl}-[4-(hydroxymethyl)thiazol-2-ylthio]acetamideHCID 67169032—

Reaction Steps

The resultant product (2.09 g) of (1-4) was dissolved in ethanol (40 mL) and tetrahydrofuran (40 mL), sodium borohydride (454 mg) was added, lithium chloride (509 mg) was further added, and the mixture was stirred at room temperature for 4.5 hrs. Water was poured into the reaction mixture, the organic solvent alone was evaporated under reduced pressure, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography using a mixed solvent of chloroform and methanol as an eluent. The solvent was evaporated from the eluent to give the title compound (1.53 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935700B2
Source datasetuspto-grants-2011_05
ORD IDord-68192e9e3f15496c865c398a31247201
Source noteuspto-grants-2011_05