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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559827Generated: October 25, 2026

2-Aminothiazole → 1-(2-Phenoxyphenyl)-5-(thiazol-2-yl)biuret

https://huagongshe.com/reaction/559827

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
ReactantBenzenamine, 2-phenoxy-HCID 75899—
ReactantDiisopropylethylamineHCID 81531—
ReactantIsocyanatocarbonyl chlorideHCID 119708—
SolventTetrahydrofuranHCID 8028—
Product1-(2-Phenoxyphenyl)-5-(thiazol-2-yl)biuretHCID 5973303555.3%

Reaction Conditions

Temperature-30 °C

Reaction Steps

To a solution of 2-phenoxyaniline (0.46 g, 2.50 mmol) in tetrahydrofuran (20 ml) was added diisopropylethylamine (0.89 ml, 5.00 mmol) and the solution was cooled to −30° C., then N-(chlorocarbonyl)isocyanate (0.3 ml, 3.75 mmol) was slowly added. The mixture was then allowed to warm up to the room temperature during 30 min. 2-Aminothiazole (0.375 g, 3.75 mmol) was added to the reaction mixture and stirred at room temperature for 6 hours. The reaction mixture was concentrated under reduced pressure to afford crude product, which was purified by silica gel chromatography (hexanes:ethyl acetate from 80:20 to 30:70) to afford title compound (0.49 g, 55%) as pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063081B2
Source datasetuspto-grants-2011_11
ORD IDord-d34249aca5d74c04a60c3bc5072a013a
Source noteuspto-grants-2011_11