Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Oxindole | HCID 321710 | — |
| Reactant | 5-Bromo-2-methoxypyridine-3-carbaldehyde | HCID 1516403 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 66917516 | HCID 66917516 | 55.5% |
Reaction Steps
To a solution of indolinone (130 mg, 0.98 mmol) in ethanol (5 mL) was added 5-bromo-2-methoxypyridine-3-carbaldehyde (J. Het. Chem, 1985, (22), 1583-1592) (200 mg, 0.98 mmol, 1 eq), followed by piperidine (0.194 mL, 1.9 mmol, 2 eq). The reaction mixture was heated at 80° C. for 2 hours and then allowed to cool to room temperature. The precipitate that formed was collected by filtration and washed with ethanol to give the title compound (180 mg, 55%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07786120B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-0ee0ad3c1fab443bba53b27ed98081dd |
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| Source note | uspto-grants-2010_08 |
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