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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545118Generated: October 29, 2026

Hydrochloric Acid → (2S)-(E)-[4-(2-carboxyethen-1-yl)thiazol-2-ylthio]-N-{[4-(3,4-dichlorobenzyl)morpholin-2-yl]methyl}acetamide

https://huagongshe.com/reaction/545118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMalonic AcidHCID 867—
ReactantPiperidineHCID 8082—
Reactant(2S)-N-{[4-(3,4-dichlorobenzyl)morpholin-2-yl]methyl}-(4-formylthiazol-2-ylthio)acetamideHCID 86616376—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
Product(2S)-(E)-[4-(2-carboxyethen-1-yl)thiazol-2-ylthio]-N-{[4-(3,4-dichlorobenzyl)morpholin-2-yl]methyl}acetamideHCID 59009139—

Reaction Conditions

Temperature100 °C

Reaction Steps

The resultant product (643 mg) of (70-2) was dissolved in pyridine (5 mL), malonic acid (291 mg) and piperidine (14 μL) were added, and the mixture was stirred at 100° C. for 3.5 hrs. The reaction mixture was poured into water, 1M hydrochloric acid was added to adjust to pH=4, 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 (618 mg) as a white amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935700B2
Source datasetuspto-grants-2011_05
ORD IDord-ca47636c2f274beab94dde1a03579a3b
Source noteuspto-grants-2011_05