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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2085490Generated: October 30, 2026

Triethylamine → N-(5-Cyclobutyl-thiazol-2-yl)-2-quinolin-6-yl-acetamide

https://huagongshe.com/reaction/2085490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPropylphosphonic anhydrideHCID 111923—
Reactant2-(Quinolin-6-yl)acetic acidHCID 11788709—
Reactant5-Cyclobutyl-1,3-thiazol-2-amineHCID 12991423—
SolventChloroformHCID 6212—
ProductN-(5-Cyclobutyl-thiazol-2-yl)-2-quinolin-6-yl-acetamideHCID 996701387.2%

Reaction Steps

A solution of 5-cyclobutyl-thiazol-2-ylamine (Preparation 2; 30 mg, 0.195 mmol) was treated with triethylamine (81 μl, 0.585 mmol), 6-quinolylaceticacid (40 mg, 0.214 mmol) and propylphosphonic acid cyclic anhydride (T3P, 126 mL, 0.214 mmol). After 2 hours, an additional 0.2 equiv. of T3P (22 μl) was added and the reaction was complete by TLC after 15 minutes. The reaction mixture was diluted with CHCl3, was washed with saturated aqu. NaHCO3, and was dried (MgSO4), filtered and concentrated in vacuo. The resulting residue was purified by silica gel chromatography (40:1 CHCl3—MeOH) to afford 55 mg of N-(5-cyclobutyl-thiazol-2-yl)-2-quinolin-6-yl-acetamide, the title compound, as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06720427B2
Source datasetuspto-grants-2004_04
ORD IDord-59f668edd1e0480d8dd2dea9b89de93f
Source noteuspto-grants-2004_04