Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 4-(ethylamino)-1H-pyrrolo[2,3-b]pyridine-5-carbaldehyde | HCID 59198499 | — |
| Reactant | 3-Cyanomethyl-5-methoxy-benzoic acid ethyl ester | HCID 59198517 | — |
| Product | HCID 178469309 | HCID 178469309 | — |
Reaction Steps
4-Ethylamino-1H-pyrrolo[2,3-b]pyridine-5-carbaldehyde (1 g, 5.3 mmol) and 3-cyanomethyl-5-methoxy-benzoic acid ethyl ester (1.3 g, 5.8 mmol) are dissolved in ethanol (4 mL) and piperidine (2 mL, 21.2 mmol) is added at room temperature. The reaction mixture is heated at 120° C. and stirred for 24 h. The reaction mixture is then concentrated and dried to yield the crude product. The crude product is used for the next step without any further purification. MS m/z 391.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07846923B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-7a9e2626e6e048858c3c9f817fa0b522 |
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| Source note | uspto-grants-2010_12 |
|---|