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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468299Generated: October 31, 2026

Aniline → HCID 86710121, compound

https://huagongshe.com/reaction/1468299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantTriethylamineHCID 8471—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86710122HCID 86710122—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 86710121HCID 86710121101%

Reaction Conditions

Temperature100 °C

Reaction Steps

2-Isopropyl-3-sulfoimidazo[1,2-a]pyridine-7-carboxylic acid (0.93 g, 3.25 mmol) obtained in step 2 was dissolved in dichloroethane (30 mL), and the solution was stirred at 100° C. for 4 hours after adding triethylamine (1.13 mL, 8.13 mmol) and phosphorus oxychloride (0.760 mL, 8.13 mmol). The reaction mixture was allowed to cool to room temperature, and stirred at room temperature for 2.5 hours after adding aniline (0.300 mL, 3.25 mmol). Then, a saturated sodium hydrogen carbonate aqueous solution was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was then evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=80/20→50/50) to give 2-isopropyl-7-phenylcarbamoylimidazo[1,2-a]pyridine-3-sulfonylchloride (1.24 g, yield 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000186B2
Source datasetuspto-grants-2015_04
ORD IDord-2602bc69a4974ac5bc0e24f517e3734e
Source noteuspto-grants-2015_04