Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 21110061 | HCID 21110061 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21110072 | HCID 21110072 | — |
Reaction Steps
0.606 cm3 (6.91 mmol) of oxalyl chloride was added, at a temperature in the region of 20° C., to 1.0 g (3.46 mmol) of 1-(quinolin-2-yl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid in suspension in 30 cm3 of dichloromethane. After stirring at a temperature in the region of 20° C. for 2 h, the reaction mixture was concentrated to dryness under reduced pressure (2.7 kPa) and the residue was used directly in the following stage.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07230007B2 |
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| Source dataset | uspto-grants-2007_06 |
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| ORD ID | ord-5c1e891c1b094060b64e1fbe0f41612c |
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| Source note | uspto-grants-2007_06 |
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