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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272949Generated: October 25, 2026

Sodium Bicarbonate → 4-[4-(3-pyrrolidin-1-ylpropoxy)phenyl]tetrahydro-2H-pyran-4-carbothioamide

https://huagongshe.com/reaction/272949

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantDiethyldithiophosphateHCID 53249491—
Reactant4-[4-(3-pyrrolidin-1-ylpropoxy)phenyl]tetrahydro-2H-pyran-4-carbonitrileHCID 59837394—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product4-[4-(3-pyrrolidin-1-ylpropoxy)phenyl]tetrahydro-2H-pyran-4-carbothioamideHCID 8660190028%

Reaction Conditions

Temperature55 °C

Reaction Steps

4-[4-(3-Pyrrolidin-1-yl-propoxy)-phenyl]-tetrahydro-pyran-4-carbonitrile (2 g, 6.4 mmol), diethyl dithiophosphate (15 mL, 8.9 mmol), and water (1.5 mL) were combined and stirred at ambient temperature for 5 hours, 55° C. for 2 hours then 70° C. for 2 hours. The reaction mixture was diluted with dichloromethane (100 mL) and basified to pH 8 with a saturated solution of NaHCO3 in water, and solid NaHCO3. The layers were separated, and further dichloromethane (100 mL) was used to extract the product. The combined organics were dried using Na2SO4, filtered and concentrated in vacuo to leave a yellow oil. The compound was purified with column chromatography on 50 g of silica, eluting with dichloromethane:methanol:ammonia (96:4:0.4) to dichloromethane:methanol:ammonia (90:10:1) to give a clear oil. The clear oil was dissolved in ethyl acetate (150 mL) and washed with 10% Na2CO3 solution. The organic layer was dried using Na2SO4, filtered and concentrated in vacuo to give the title compound as a white solid (0.61 g, 28%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456164B2
Source datasetuspto-grants-2008_11
ORD IDord-5a70f34275684bb29dfa9b32eca1be85
Source noteuspto-grants-2008_11