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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492199Generated: October 29, 2026

Oxalyl chloride → HCID 86596415, compound

https://huagongshe.com/reaction/492199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant1-(Isoquinolin-3-yl)-1H-indole-3-carboxylic acidHCID 68971637—
SolventDichloromethaneHCID 6344—
ProductHCID 86596415HCID 8659641579.4%

Reaction Conditions

Temperature22 °C

Reaction Steps

0.7 cm3 (8 mmol) of oxalyl chloride is added to a suspension, cooled to a temperature in the region of 5° C., of 0.74 g (2.57 mmol) of 3-carboxy-1-(isoquinol-3-yl)-1H-indole in 15 cm3 of dichloromethane under an argon atmosphere. After stirring at a temperature in the region of 22° C. for 15 hours, the reaction mixture is concentrated to dryness under reduced pressure (2.7 kPa). The residue, dissolved in 15 cm3 of dichloromethane, is again reacted with 1 cm3 (11.46 mmol) of oxalyl chloride. After stirring at a temperature in the region of 22° C. for 48 hours, the reaction mixture is concentrated to dryness under reduced pressure (2.7 kPa) to give 0.7 g of 3-chlorocarbonyl-1-(isoquinol-3-yl)-1H-indole hydrochloride in the form of a yellow solid which is used directly in the following step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531663B2
Source datasetuspto-grants-2009_05
ORD IDord-c20c21c92a734c868e84b994c10a1e0e
Source noteuspto-grants-2009_05