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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269776Generated: October 30, 2026

Sodium Bicarbonate → HCID 68458639, compound

https://huagongshe.com/reaction/269776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantPyridinium chlorideHCID 10176127—
Reactant3-chloro-4-(1-methyl-1H-imidazol-2-ylsulfanyl)phenylamineHCID 11459088—
ReactantHCID 68460168HCID 68460168—
SolventGlycol monoethyl etherHCID 8076—
ProductHCID 68458639HCID 6845863960.9%

Reaction Conditions

Temperature105 °C

Reaction Steps

A mixture of 0.5 g (1.45 mmol) of 4-chloro-6-nitro-7-(4-pyrrolidin-1-ylpiperidin-1-yl)quinoline-3-carbonitrile, 0.38 g (1.6 mmol) of 3-chloro-4-[(1-methyl-1H-imidazole-2-yl)sulfanyl]aniline and 0.17 g of pyridine hydrochloride in 7.0 mL of 2-ethoxyethanol is heated at 105° C. for 1 hour. After cooling to room temperature, the mixture is stirred with 15 mL of saturated solution of sodium bicarbonate. The resulting solid is collected by filtration and washed with water. Some of the product dissolves in water, which is recovered by extracting the aqueous layer with solution of 95:5 methylene chloride/methanol. The organic layer is evaporated to provide crude product. The combined solids are purified by silica gel chromatography (gradient 95:5methylene chloride/methanol to 4:1 methylene chloride/methanol) gives 0.52 g of 4-({3-chloro-4-[(1-methyl-1H-imidazole-2-yl)thio]phenyl}amino)-6-nitro-7-(4-pyrrolidin-1-ylpiperidin-1-yl)quinoline-3-carbonitrile as an orange solid, mp 220-230° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07449460B2
Source datasetuspto-grants-2008_11
ORD IDord-7f42b46e2a5c405d9a302493f1e13a8d
Source noteuspto-grants-2008_11