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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1978934Generated: November 3, 2026

HCID 178522937, compound → HCID 178522938, compound

https://huagongshe.com/reaction/1978934

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178522937HCID 178522937—
CatalystPalladiumHCID 23938—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 178522938HCID 17852293827.4%

Reaction Steps

A solution of N-(4-chlorobenzyl)-4-hydroxy-2-(3-hydroxy-1-propynyl)-thieno[2,3-b]pyridine-5-carboxamide (Example No.5) (0.300 g) in 1/1 CH2Cl2/CH3OH (70 mL) is hydrogenated over 10% Pd/C (90 mg) at 35 psi. After 3 h, an additional 90 mg of 10% Pd/C is added, and the solution is hydrogenated at 35 psi for 1 h. The reaction mixture is filtered through a Celite pad, and the filtrate is concentrated in vacuo. The resulting pale orange solid is purified via column chromatography (CH2Cl2:CH3OH; 98:2, 95:5). Fractions homogeneous by TLC are combined and concentrated in vacuo to yield and off-white solid which is recrystallized from ethanol to yield 0.083 g (27%) of the title compound as a white, crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06239142B1
Source datasetuspto-grants-2001_05
ORD IDord-a99f78b9439345e79501c0de3ff77f24
Source noteuspto-grants-2001_05