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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2218513Generated: October 24, 2026

Diisopropylethylamine → 1-Acetyl-N-(3-(N-(4-(benzofuran-2-yl)thiazol-2-yl)thiophene-2-carboxamido)propyl)piperidine-4-carboxamide

https://huagongshe.com/en/reaction/2218513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Acetylpiperidine-4-carbonyl chlorideHCID 100950—
ReactantN-(3-aminopropyl)-N-(4-(benzofuran-2-yl)thiazol-2-yl)thiophene-2-carboxamideHCID 68407996—
SolventChloroformHCID 6212—
Product1-Acetyl-N-(3-(N-(4-(benzofuran-2-yl)thiazol-2-yl)thiophene-2-carboxamido)propyl)piperidine-4-carboxamideHCID 68406261—

Reaction Steps

A mixture of the amine prepared above (77 mg, 0.2 mmol) and N,N-diisopropylethylamine (139 μL, 0.8 mmol) was dissolved in chloroform (2 mL), and a portion of the solution (200 μL, 0.02 mmol) was added to a solution of 1-acetyl-isonipecotoyl chloride (7.6 mg, 0.04 mmol) in chloroform (200 μL). The reaction mixture was maintained at room temperature overnight.). The reaction mixture was maintained at room temperature overnight, then concentrated in vacuo. The resulting residue was dissolved in DMSO (200 μL) and subjected to HPLC purification (Method Z) to provide the title compound (4.5 mg) as a yellowish solid. LC/MS (ESI) m/z 537.1 [M+H]. HPLC retention time (Method C)=3.44 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07410988B2
Source datasetuspto-grants-2008_08
ORD IDord-4dfe5492e5094c07ae111d76eb72d2ae
Source noteuspto-grants-2008_08