Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 1-(Quinolin-5-yl)-1H-pyrrole-3-carboxylic acid | HCID 22024967 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22024994 | HCID 22024994 | 106.6% |
Reaction Steps
0.5 mL (5.73 mmol) of oxalyl chloride is added to a solution, cooled to a temperature in the region of 5° C., of 0.42 g (1.76 mmol) of 3-carboxy-1-(quinol-5-yl)-1H-pyrrole in 10 mL of dichloromethane under an argon atmosphere. After stirring at a temperature in the region of 22° C. for 15 hours, concentrating the reaction mixture to dryness under reduced pressure (2.7 kPa) gives 0.55 g of 3-chlorocarbonyl-1-(quinol-5-yl)-1H-pyrrole hydrochloride in the form of a cream-coloured solid which is used directly in the following step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07078414B2 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-9c1ae5b007ce40f89648f68658dddefe |
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| Source note | uspto-grants-2006_07 |
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