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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23660Generated: October 29, 2026

Diisopropylethylamine → HCID 10218486, compound

https://huagongshe.com/reaction/23660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantN-{4-[1-hydroxy-2-(methylamino)ethyl]phenyl}acetamideHCID 10171338—
ReactantN-(4-chlorobenzyl)-2-(chloromethyl)-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamideHCID 22574363—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 10218486HCID 1021848678.7%

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 (50 mg, 0.13 mmol), N-{4-[1-hydroxy-2-(methylamino)ethyl]phenyl}acetamide (Preparation 56)(42 mg, 0.20 mmol) and diisopropylethylamine (35 μL, 0.20 mmol) in dry DMF (2.7 mL) was heated to 60° C., becoming a solution. The reaction was stirred for 7 hours at that temperature. After cooling to room temperature, the solution was diluted with water (7 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/DMF/water (5 mL/2 drops/1 mL, dissolved with warming, added water and then cooled to 0° C. overnight) gave the title compound (58 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06852731B2
Source datasetuspto-grants-2005_02
ORD IDord-fc5081e0a219480384868562ebfcd079
Source noteuspto-grants-2005_02