Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 4-oxo-4,5,6,7-tetrahydro-2H-pyrrolo[3,4-c]pyridine-1-carbaldehyde | HCID 9964189 | — |
| Reactant | HCID 18414718 | HCID 18414718 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 69707470 | HCID 69707470 | — |
Reaction Steps
A mixture of 5-(morpholine-4-carbonyl)-1,3-dihydro-indol-2-one (49.2 mg, 0.2 mmol), 4-oxo-4,5,6,7-tetrahydro-2H-pyrrolo[3,4-c]pyridine-1-carbaldehyde (1 eq.) and 0.1 mL of piperidine in ethanol (1 mL) was heated in a sealed tube at 80° C. for 3 hours. The precipitate was collected by vacuum filtration, washed with ethanol and dried to give the title compound as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06465507B2 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-ab6ab0087da7407d80023389a5c55446 |
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| Source note | uspto-grants-2002_10 |
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