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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509707Generated: October 30, 2026

HCID 59455235, compound → HCID 57875913, compound

https://huagongshe.com/reaction/509707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59455235HCID 59455235—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 57875913HCID 5787591326.1%

Reaction Steps

2,3,4,5-tetrahydro-2,8-dimethyl-5-(3-(pyridin-2-yl)prop-2-ynyl)-1H-pyrido[4,3-b]indole (See Example 61A) (20 mg, 0.06 mmol) was hydrogenated in methanol (2 ml) with 10% Pd—C (10 mg) at 1 atm of hydrogen to obtain 5 mg of 2,3,4,5-tetrahydro-2,8-dimethyl-5-(3-(pyridin-2-yl)propyl)-1H-pyrido[4,3-b]indole after purification on neutral alumina chromatography eluting with methanol-dichloromethane gradient. The free base was converted into its diHCl salt by treatment of ethanolic HCl.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096591B2
Source datasetuspto-grants-2015_08
ORD IDord-f7f7011f8d93412a90ccfdba6119c0a9
Source noteuspto-grants-2015_08