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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399536Generated: October 31, 2026

Triethylamine → HCID 15232777, compound

https://huagongshe.com/reaction/2399536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrifluoromethanesulfonic acidHCID 62406—
Reactant4,5-Bis(4-methoxyphenyl)-1,3-thiazol-2-amineHCID 1481725—
SolventChloroformHCID 6212—
ProductHCID 15232777HCID 1523277726.7%

Reaction Steps

13.5 g of anhydrous trifluoromethanesulfonic acid was slowly dropped into a solution of 5.0 g of 2-amino-4,5-bis(4-methoxyphenyl)thiazole and 5.0 ml of triethylamine in chloroform under stirring in a nitrogen atmosphere at -20° to -15° C., and the resulting mixture was stirred as such for 2 hours. Then the reaction mixture was successively washed with diluted hydrochloric acid, a saturated aqueous solution of sodium hydrogencarbonate and water in this order and dried over anhydrous magnesium sulfate. After distilling off the solvent under reduced pressure, the reaction product was separated with a silica gel column by using chloroform/ethyl acetate as a developer. The crystals thus obtained were recrystallized from isopropyl ether/ethyl acetate to give 1.9 g of 2-trifluoromethanesulfonylamino-4,5-bis(4-methoxy-phenyl)thiazole. The melting point of this product was from 240° to 242° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05449783
Source datasetuspto-grants-1995_09
ORD IDord-f11e6a150b6b439c86c140e057d3d1a2
Source noteuspto-grants-1995_09