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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1971006Generated: November 1, 2026

1-[(2-Hydroxy-1,2-dimethylpropyl)amino]-7-(pyridin-3-ylethynyl)-5H-pyrido[4,3-b]indole-4-carboxamide → 1-[(2-Hydroxy-1,2-dimethylpropyl)amino]-7-(2-pyridin-3-ylethyl)-5H-pyrido[4,3-b]indole-4-carboxamide

https://huagongshe.com/reaction/1971006

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[(2-Hydroxy-1,2-dimethylpropyl)amino]-7-(pyridin-3-ylethynyl)-5H-pyrido[4,3-b]indole-4-carboxamideHCID 59543163—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1-[(2-Hydroxy-1,2-dimethylpropyl)amino]-7-(2-pyridin-3-ylethyl)-5H-pyrido[4,3-b]indole-4-carboxamideHCID 42636046—

Reaction Steps

Hydrogen was bubbled through a solution of 1-[(2-hydroxy-1,2-dimethylpropyl)amino]-7-(pyridin-3-ylethynyl)-5H-pyrido[4,3-b]indole-4-carboxamide (10 mg, 0.024 mmol) and Pd/C (10%, 2.6 mg) in EtOH (1.3 mL). After complete conversion, the mixture was purged with nitrogen, filtered through a pad of Celite, and concentrate to afford the title compound. LRMS (APCI) calc'd for (C24H27N5O2) [M+H]+, 418.2. found 418.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431569B2
Source datasetuspto-grants-2013_04
ORD IDord-f261eab483834958bc6a3db1a4d739c9
Source noteuspto-grants-2013_04