HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404610Generated: October 26, 2026
Benzaldehyde → tert-butyl 4-[4-[1-[(E)-benzylideneamino]pyrrolo[3,2-b]pyridin-6-yl]pyrazol-1-yl]piperidine-1-carboxylate
https://huagongshe.com/reaction/1404610
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | tert-butyl 4-[4-(1-amino-1H-pyrrolo[3,2-b]pyridin-6-yl)-1H-pyrazol-1-yl]piperidine-1-carboxylate | HCID 58532283 | — |
| Product | tert-butyl 4-[4-[1-[(E)-benzylideneamino]pyrrolo[3,2-b]pyridin-6-yl]pyrazol-1-yl]piperidine-1-carboxylate | HCID 58532304 | 81% |
Reaction Steps
A mixture of tert-butyl 4-[4-(1-amino-1H-pyrrolo[3,2-b]pyridin-6-yl)-1H-pyrazol-1-yl]piperidine-1-carboxylate (30 mg, 0.078 mmol) and benzaldehyde (2.0 mL, excess) was heated to 60° C. for 10 min. Heptanes (4.0 ml) was added and the mixture was heated to reflux for 10 min. The product was purified by column chromatography (EtOAc:MeOH=100:5) and the entitled intermediate was isolated as a white solid (30 mg, 81% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08912330B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-3121fc37c0dd4e8aba7074080af75f0a |
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| Source note | uspto-grants-2014_12 |
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