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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23669Generated: October 29, 2026

Diisopropylethylamine → N-(4-chlorobenzyl)-2-{[[2-hydroxy-2-(4-morpholin-4-ylphenyl)ethyl](methyl)amino]methyl}-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamide

https://huagongshe.com/reaction/23669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(Methylamino)-1-(4-morpholin-4-ylphenyl)ethanol dihydrochlorideHCID 22574359—
ReactantN-(4-chlorobenzyl)-2-(chloromethyl)-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamideHCID 22574363—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductN-(4-chlorobenzyl)-2-{[[2-hydroxy-2-(4-morpholin-4-ylphenyl)ethyl](methyl)amino]methyl}-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamideHCID 1015322551.1%

Reaction Steps

A mixture of N-(4-chlorobenzyl)-2-(chloromethyl)-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamide (100 mg, 0.25 mmol), 2-(methylamino)-1-(4-morpholin-4-ylphenyl)ethanol dihydrochloride (Preparation 89) (118 mg, 0.38 mmol) and diisopropylethylamine (180 μL, 1.0 mmol) in dry DMF (5.0 mL) was stirred for 48 hours at room temperature. The solution was diluted with water (10 mL). The resulting milky suspension was stirred vigorously for 30 minutes, and then left standing overnight at room temp. The mixture was filtered, and the collected solid was washed with water and dried in vacuo, leaving a white solid. Recrystallization from acetonitrile (10 mL, dissolved with warming and then cooled to 0° C. overnight) gave the title compound (76 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06852731B2
Source datasetuspto-grants-2005_02
ORD IDord-ed6d8608a7274efa80fb323a24775399
Source noteuspto-grants-2005_02