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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604584Generated: October 30, 2026

Hydrochloric Acid → HCID 67039194, compound

https://huagongshe.com/reaction/604584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantHCID 67039644HCID 67039644—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 67039194HCID 6703919485%

Reaction Conditions

Temperature0 °C

Reaction Steps

To 4-[3-(2,2-dimethylpropionyl)-2-phenyl-5-(2-phenylpropionylamino)-2,3-dihydro-1,3,4-thiadiazol-2-yl]-N-(2-hydroxyethyl)butanamide (1.21 g, 2.31 mmol) obtained in Step 4 mentioned above was added dichloromethane (20 mL), and the mixture was stirred at 0° C. Then, to the mixture were added pyridine (0.470 mL, 5.77 mmol) and tert-butyldimethylsilyl chloride (869 mg, 5.77 mmol), and the mixture was stirred at room temperature for 3 hours. To the mixture were added 1 mol/L hydrochloric acid (20 mL) and water (30 mL), and the mixture was extracted with chloroform. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. To the resulting residue was added diisopropyl ether, and the deposited white solid was collected by filtration. The resulting solid was washed with water and diisopropyl ether, and dried under reduced pressure to give N-[2-(tert-butyldimethylsiloxy)ethyl]-4-[3-(2,2-dimethylpropionyl)-2-phenyl-5-(2-phenylpropionylamino)-2,3-dihydro-1,3,4-thiadiazol-2-yl]butanamide (1.25 g, 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910611B2
Source datasetuspto-grants-2011_03
ORD IDord-c56a1b19851540c98b86e593a92a296d
Source noteuspto-grants-2011_03