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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839889Generated: October 31, 2026

Pyridine → HCID 69878105, compound

https://huagongshe.com/reaction/1839889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPotassium IodideHCID 4875—
ReactantEthyl 2-bromopropionateHCID 79040—
ReactantHCID 178426791HCID 178426791—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69878105HCID 6987810545%

Reaction Steps

1.0 Gram (2.7 mmol) of the 4,4,5,8-tetramethyl-6-(1,3-dimethyl-5-hydroxypyrazol-4-yl)carbonylthiochroman-1,1-dioxide obtained in Preparation Example 6 was dissolved in 10 ml of tetrahydrofuran, and further, 0.27 g (3.5 mmol) of pyridine and 90 mg of potassium iodide were added. Then, 0.63 g (3.5 mmol) of ethyl 2-bromopropionate was added, and the mixture was refluxed under heat for 7 hours. The reaction mixture was cooled to room temperature, and the solvent was distilled off under reduced pressure. The resultant residue was extracted by adding ethyl acetate, and the extract was consecutively washed with 10% hydrochloric acid, with a saturated sodium bicarbonate aqueous solution and with a saturated sodium chloride aqueous solution, and the solvent was distilled off under reduced pressure to give 0.57 g (yield 45%) of 4,4,5,8-tetramethyl-6-(1,3-dimethyl-5-(1-ethoxycarbonyl)ethoxypyrazol-4-yl)carbonylthiochroman-1,1-dioxide (Compound No. 40).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677460B1
Source datasetuspto-grants-2004_01
ORD IDord-339a1fe02c8548ab91c3807e9995aa1a
Source noteuspto-grants-2004_01