Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23686Generated: October 28, 2026

Diisopropylethylamine → HCID 10311790, compound

https://huagongshe.com/reaction/23686

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantN-(4-chlorobenzyl)-2-(chloromethyl)-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamideHCID 22574363—
Reactant1-(6-Methoxypyridin-3-yl)-2-(methylamino)ethanol dihydrochlorideHCID 22574369—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 10311790HCID 1031179063.6%

Reaction Conditions

Temperature60 °C

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), 1-(6-methoxypyridin-3-yl)-2-(methylamino)ethanol dihydrochloride (Preparation 52) (97 mg, 0.38 mmol) and diisopropylethylamine (199 μL, 1.2 mmol) in dry DMF (5 mL) was heated to 60° C., becoming a solution. The reaction was stirred for 6 hours at that temperature. After cooling to room temperature, the solution was diluted with water (15 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 (86 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06852731B2
Source datasetuspto-grants-2005_02
ORD IDord-9a38a45072e2457dadf539f7f9ca3d9c
Source noteuspto-grants-2005_02