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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718234Generated: October 30, 2026

Triethylamine → 2-(4-Chlorophenoxy)-1-(4-(2-(4-fluorophenyl)-5-methylthiazolo[5,4-d]pyrimidin-7-yl)piperazin-1-yl)ethanone

https://huagongshe.com/reaction/718234

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-(4-Chlorophenoxy)-1-(piperazin-1-yl)ethanoneHCID 1074760—
Reactant7-Chloro-2-(4-fluorophenyl)-5-methylthiazolo[5,4-d]pyrimidineHCID 86662439—
Solvent1,4-DioxaneHCID 31275—
Product2-(4-Chlorophenoxy)-1-(4-(2-(4-fluorophenyl)-5-methylthiazolo[5,4-d]pyrimidin-7-yl)piperazin-1-yl)ethanoneHCID 4691647875%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 7-chloro-2-(4-fluorophenyl)-5-methylthiazolo[5,4-d]pyrimidine (30 mg, 0.11 mmol) and triethylamine (22 μl, 0.16 mmol) in dioxane (1 ml) was added 2-(4-chlorophenoxy)-1-(piperazin-1-yl)ethanone (38 mg, 0.16 mmol). The reaction mixture was heated at 70° C. for 3 hours. After cooling, the volatiles were removed under reduced pressure. The crude residue was purified by chromatography on silica gel (CH2Cl2/MeOH 70:1) to yield the title compound as a white solid (40 mg, 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193741B2
Source datasetuspto-grants-2015_11
ORD IDord-dcddfdca619d46f38aa6bfcbbcc1fc4e
Source noteuspto-grants-2015_11