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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243514Generated: October 30, 2026

Cyclopentane-1,1-diacetic anhydride → 2-(1-((3-(3-(5,6,7,8-Tetrahydro-1,8-naphthyridin-2-yl)propyl)-1,2,4-oxadiazol-5-yl)methyl)cyclopentyl)acetic acid

https://huagongshe.com/reaction/1243514

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentane-1,1-diacetic anhydrideHCID 79743—
ReactantN'-hydroxy-4-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)butanimidamideHCID 21927918—
Solvent1,4-DioxaneHCID 31275—
Product2-(1-((3-(3-(5,6,7,8-Tetrahydro-1,8-naphthyridin-2-yl)propyl)-1,2,4-oxadiazol-5-yl)methyl)cyclopentyl)acetic acidHCID 10228662—

Reaction Conditions

Temperature100 °C

Reaction Steps

A stirred mixture of (1Z)-N′-hydroxy-4-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)butanimidamide (100 mg, WO 99/30709), 3,3-tetramethyleneglutaric anhydride (80 mg, Aldrich) and 1,4-dioxane (2 mL, Aldrich) was heated to 100° C. for 16 hrs. The resulting mixture was purified by HPLC to provide the title compound as a gum. 1H (CD3OD) δ 1.68 (8H, m); 1.95 (2H, p); 2.13 (2H, p); 2.45 (2H, s); 2.80 (6H, m); 3.15 (2H, s); 3.50 (2H, t); 6.63 (1H, d);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07119098B2
Source datasetuspto-grants-2006_10
ORD IDord-ea7b0ab4331440c6bf7787e20ac15b34
Source noteuspto-grants-2006_10