Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 883523Generated: October 27, 2026

Water → 3-(Phenylsulfonyl)-8-quinolinamine

https://huagongshe.com/reaction/883523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthylenediaminetetraacetic AcidHCID 6049—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(Benzenesulfonyl)-8-nitroquinolineHCID 53425503—
Catalysttitanium(III) trichlorideHCID 10313229—
SolventHydrochloric AcidHCID 313—
SolventTetrahydrofuranHCID 8028—
Product3-(Phenylsulfonyl)-8-quinolinamineHCID 5342550272%

Reaction Steps

A slurry of 8-nitro-3-phenylsulfonylquinoline (D4) (46.7 g, 172 mmol), in tetrahydrofuran (750 ml) was added to a stirred solution of 30% titanium (III) chloride in aqueous HCl (470 ml) [Supplied by BDH] cooled in an ice bath, at such a rate that the temperature was maintained below 35° C. Once the addition was completed, the solution was stirred for a further 10 minutes then water (1.5 L) was introduced and the mixture poured into a 5 L beaker. The rapidly stirred solution was treated by portionwise addition of solid potassium carbonate in order to attain pH ˜8.5. EDTA (250 g, 0.86 mol) was added and followed by further potassium carbonate to maintain pH ˜8.5. The mixture was extracted with dichloromethane (3×1 L) and the combined organic phase passed through a silica plug (500 g) eluting with further dichloromethane (1 L) and 10% ethyl acetate in dichloromethane (1 L). The combined organic phases were evaporated and the residue subjected to purification using Biotage Flash-75 chromatography apparatus (2 kg silica gel), eluting with dichloromethane and increasing proportions of ether to give the title compound (D5) (34.5 g, 72%) as a pale brown solid;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08236947B2
Source datasetuspto-grants-2012_08
ORD IDord-8d43f73dc91243a2965cb7a1ad264069
Source noteuspto-grants-2012_08