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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1671780Generated: November 1, 2026

Potassium Carbonate → 6-(4-(4-Fluorophenyl)oxazol-5-yl)benzo[d]thiazol-2-amine

https://huagongshe.com/reaction/1671780

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanta-Tosyl-(4-fluorobenzyl) isocyanideHCID 10827289—
Reactant2-Aminobenzo[d]thiazole-6-carbaldehydeHCID 13821541—
SolventEthanolHCID 702—
Product6-(4-(4-Fluorophenyl)oxazol-5-yl)benzo[d]thiazol-2-amineHCID 5752715786.1%

Reaction Steps

A solution of 2-aminobenzo[d]thiazole-6-carbaldehyde (0.91 g, 5.11 mmol, 1.0 eq.), 1-((4-fluorophenyl)(isocyano)methylsulfonyl)-4-methylbenzene (2.20 g, 7.60 mmol, 1.5 eq.), and K2CO3 (1.34 g, 9.70 mmol, 1.9 eq.) in EtOH (51 mL) was refluxed for 4 h. After cooling to room temperature, the reaction mixture was concentrated in vacuo, and the residue was taken up in CH2Cl2 and saturated aqueous NaHCO3. After separation of the layers, the aqueous layer was extracted with CH2Cl2 (2×). The organic layers were combined, dried over Na2SO4, filtered, and concentrated in vacuo. Silica gel chromatography using CH2Cl2:MeOH (40:1) as eluent afforded 6-(4-(4-fluorophenyl)oxazol-5-yl)benzo[d]thiazol-2-amine as a tan solid (1.37 g, 86% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994337B2
Source datasetuspto-grants-2011_08
ORD IDord-f567ecc4a9ba41a38ff52e6d75de2a76
Source noteuspto-grants-2011_08