Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 69055087 | HCID 69055087 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 45790884 | HCID 45790884 | 126% |
Reaction Steps
1.3 ml (10.4 mmol) of oxalyl chloride were dissolved in 60 ml of CH2Cl2. The solution was cooled at −10° C. and 3.0 g (14.4 mmol) of 2-(4-pyridyl)quinoline-4-carboxylic acid hydrochloride were added portionwise. The reaction mixture was left 72 hours at room temperature and then evaporated to dryness to yield 4.0 g of the title compound, used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07482458B2 |
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| Source dataset | uspto-grants-2009_01 |
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| ORD ID | ord-2608ab854c8141b4b26baa8712daf0ac |
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| Source note | uspto-grants-2009_01 |
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