HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492199Generated: October 29, 2026
Oxalyl chloride → HCID 86596415, compound
https://huagongshe.com/reaction/492199
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 1-(Isoquinolin-3-yl)-1H-indole-3-carboxylic acid | HCID 68971637 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86596415 | HCID 86596415 | 79.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07531663B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-c20c21c92a734c868e84b994c10a1e0e |
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| Source note | uspto-grants-2009_05 |
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