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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071347Generated: November 4, 2026

N-(1-tert-Butoxycarbonyl-1H-pyrrolo[2,3-b]pyridin-4-yl)-1-benzyloxycarbonyl-4-piperidinecarboxamide → N-(1-tert-butoxycarbonyl-1H-pyrrolo[2,3-b]pyridin-4-yl)-4-piperidinecarboxamide

https://huagongshe.com/reaction/1071347

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(1-tert-Butoxycarbonyl-1H-pyrrolo[2,3-b]pyridin-4-yl)-1-benzyloxycarbonyl-4-piperidinecarboxamideHCID 22393147—
CatalystHCID 178420936HCID 178420936—
SolventMethanolHCID 887—
ProductN-(1-tert-butoxycarbonyl-1H-pyrrolo[2,3-b]pyridin-4-yl)-4-piperidinecarboxamideHCID 2239316783.4%

Reaction Steps

N-(1-tert-Butoxycarbonyl-1H-pyrrolo[2,3-b]pyridin-4-yl)-1-benzyloxycarbonyl-4-piperidinecarboxamide (2 g) was dissolved in methanol (30 ml) and 10% palladium carbon hydroxide (0.5 g) was added for hydrogenation (normal pressure). After the completion of the reaction, the catalyst was filtered off and the filtrate was concentrated under reduced pressure to give 1.2 g of N-(1-tert-butoxycarbonyl-1H-pyrrolo[2,3-b]pyridin-4-yl)-4-piperidinecarboxamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06906061B2
Source datasetuspto-grants-2005_06
ORD IDord-dd95bfe954d14bffbc864db4794da3df
Source noteuspto-grants-2005_06