HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269776Generated: October 30, 2026
Sodium Bicarbonate → HCID 68458639, compound
https://huagongshe.com/reaction/269776
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Pyridinium chloride | HCID 10176127 | — |
| Reactant | 3-chloro-4-(1-methyl-1H-imidazol-2-ylsulfanyl)phenylamine | HCID 11459088 | — |
| Reactant | HCID 68460168 | HCID 68460168 | — |
| Solvent | Glycol monoethyl ether | HCID 8076 | — |
| Product | HCID 68458639 | HCID 68458639 | 60.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07449460B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-7f42b46e2a5c405d9a302493f1e13a8d |
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| Source note | uspto-grants-2008_11 |
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