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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 265014Generated: October 28, 2026

Potassium Hydroxide → Ammonia

https://huagongshe.com/reaction/265014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantThionyl ChlorideHCID 24386—
Reactant(R)-8-fluoro-5-carboxy-3-(N-3-pentyl-N-n-propylamino)chromanHCID 53656554—
Reactant(R)-8-Fluoro-5-methoxycarbonyl-3-(N-3-pentyl-N-n-propylamino)chromanHCID 53912065—
CatalystDimethylformamideHCID 6228—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductAmmoniaHCID 222—
Product(R)-5-Carbamoyl-8-Fluoro-3-(N-3-pentyl-N-n-propylamino)chromanHCID 22853658—

Reaction Steps

(R)-8-Fluoro-5-methyloxycarbonyl-3-(N-3-pentyl-N-n-propylamino)chroman (0.72 g, 2.13 mmol) was hydrolysed with KOH (0.20 g, 3.1 mmol) in 20 ml MeOH and 10 ml H2O, under reflux conditions for 20 hours and gave after evaporation, and co-evaporation with toluene, (R)-8-fluoro-5-carboxy-3-(N-3-pentyl-N-n-propylamino)chroman as a white solid. SOCl2 (0.8 ml, 11 mmol) was added to a slurry of (R)-8-fluoro-5-carboxy-3-(N-3-pentyl-N-n-propylamino)chroman in 50 ml dry CH2Cl2 and 1 drop DMF (catalytic amount). After reflux for 2 hours, the slurry was evaporated, and the residue, dissolved in 10 ml dry THF was added dropwise to 35 ml ice-cooled conc. NH3 under stirring. The THF was evaporated after 2 hours and extraction with EtOAc×2, drying (Na2SO4) and evaporation gave 0.51 g of a crude product. Purification by flash chromatography with hexane:EtOAc:NH3, (60:40:0.5) gave 0.41 g of (R)-5-carbamoyl-8-fluoro-3-(N-3-pentyl-N-n-propylamino)chroman as light yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646309
Source datasetuspto-grants-1997_07
ORD IDord-4ef6489c496c4c1691378df505ccfa94
Source noteuspto-grants-1997_07