Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23647Generated: October 29, 2026

Sodium Bicarbonate → 2-{[[2-(1-Benzofuran-2-yl)-2-hydroxyethyl](methyl)amino]methyl}-N-(4-chlorobenzyl)-3-(hydroxymethyl)-4-methyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamide

https://huagongshe.com/reaction/23647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant2-{[[2-(1-benzofuran-2-yl)-2-hydroxyethyl](methyl)amino]methyl}-N-(4-chlorobenzyl)-4-methyl-7-oxo-3-{[2-(trimethylsilyl)ethoxy]methyl}-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamideHCID 22574328—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
Product2-{[[2-(1-Benzofuran-2-yl)-2-hydroxyethyl](methyl)amino]methyl}-N-(4-chlorobenzyl)-3-(hydroxymethyl)-4-methyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamideHCID 2257440878.7%

Reaction Steps

A solution of 154 mg of 2-{[[2-(1-benzofuran-2-yl)-2-hydroxyethyl](methyl)amino]methyl}-N-(4-chlorobenzyl)-4-methyl-7-oxo-3-{[2-(trimethylsilyl)ethoxy]methyl}-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamide in 3 mL of 75% TFA in CH2Cl2 is stirred at room temperature for 4 h, then diluted with CHCl3 and added to stirred aq. NaHCO3. The aqueous phase is extracted with 4 portions of CH2Cl2, and the combined organic phases dried (Na2SO4) and concentrated under reduced pressure. Flash chromatography of the residue on silica gel using 4% MeOH in CH2Cl2 provides 103 mg of the title compound as a pale yellow solid. Recrystallization from acetonitrile affords white needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06852731B2
Source datasetuspto-grants-2005_02
ORD IDord-89fbb84a9e0d4acea2bc7a58057f2492
Source noteuspto-grants-2005_02