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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280686Generated: October 30, 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/1280686

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 numberUS06451825B1
Source datasetuspto-grants-2002_09
ORD IDord-4057c07d2f804e0b9be43aabd02c273f
Source noteuspto-grants-2002_09