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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468302Generated: November 1, 2026

Triethylamine → HCID 86710134, compound

https://huagongshe.com/reaction/1468302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantTrimethylsilyl chlorosulphateHCID 78059—
ReactantHCID 82388494HCID 82388494—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 86710134HCID 8671013493%

Reaction Conditions

Temperature90 °C

Reaction Steps

7-Bromo-2-isopropylimidazo[1,2-a]pyridine (1.00 g, 4.18 mmol) obtained in step 1 of Example 28 was dissolved in 1,2-dichloroethane (10 mL). Under ice-cooled condition, trimethylsilyl chlorosulfonate (1.20 mL, 8.36 mmol) was added, and the mixture was stirred at 90° C. for 3 hours. Under ice-cooled condition, triethylamine (1.17 mL, 8.36 mmol) and phosphoryl chloride (0.779 mL, 8.36 mmol) were added, and the mixture was stirred at 100° C. for 1.5 hours. The solvent was evaporated under reduced pressure, and the residue was dissolved in acetonitrile. After adding a sodium hydrogen carbonate aqueous solution, the precipitated solid was collected by filteration to give 7-bromo-2-isopropylimidazo[1,2-a]pyridine-3-sulfonylchloride (1.31 g, yield 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000186B2
Source datasetuspto-grants-2015_04
ORD IDord-0012150464644208a979308b18590fec
Source noteuspto-grants-2015_04