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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291944Generated: November 1, 2026

Dimethyl Sulfoxide → HCID 14326854, compound

https://huagongshe.com/reaction/2291944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantDichloromethaneHCID 6344—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 21278405HCID 21278405—
SolventTriethylamineHCID 8471—
ProductHCID 14326854HCID 1432685489%

Reaction Conditions

Temperature-55 °C

Reaction Steps

To 100 ml of a dried dichloromethane solution containing 2.67 g of oxalyl chloride was added dropwise at -50° C. 20 ml of a dichloromethane solution containing 1.64 g of dimethylsulfoxide. The mixture was allowed to stand for 5 minutes. To the mixture was added dropwise over a period of 10 minutes, while maintaining the temperature at -55° C., 40 ml of a dried dichloromethane solution containing 5.84 g of 1-(5-isoquinolinesulfonyl)-4-hydroxypiperidine as obtained in Example 7, followed by stirring at that temperature for 20 minutes. To the resulting mixture was added 1.4 ml of triethylamine, and the mixture was stirred for 5 minutes. Then, the temperature of the mixture was raised to 15° C. The mixture was washed twice with 100 ml each of water and dried with anhydrous sodium sulfate. Then, the dichloromethane was removed under reduced pressure to obtain a residue. The residue thus obtained was subjected to purification by silica gel column chromatography (Wacogel C-200, 150 g; solvent: chloroform) to obtain 5.16 g of 1-(5-isoquinolinesulfonyl)-4-piperidone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04798897
Source datasetuspto-grants-1989_01
ORD IDord-20543cc4eb884a5aa5e1b520c34a3340
Source noteuspto-grants-1989_01