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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418438Generated: October 25, 2026

Ethyl chloroformate → HCID 178526847, compound

https://huagongshe.com/reaction/1418438

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
Reactant2-Bromo-5-nitrothiazoleHCID 18211—
Reactant3-Amino-1-(2-(trifluoromethyl)phenyl)thioureaHCID 723187—
Reactant2-(Trifluoromethyl)phenyl isothiocyanateHCID 737162—
ReactantHCID 178518949HCID 178518949—
ProductHCID 178526847HCID 17852684725.8%

Reaction Steps

The title compound was prepared in a manner similar to that described in Example 5 starting with 2-(trifluoromethyl) phenyl isothiocyanate. The intermediate 4-[2-(trifluoromethyl)phenyl]-3-thiosemicarbazide (2.04 g) was treated with ethyl chloroformate (1.09 g) as in example 5. The reaction product 3-hydroxy-5-mercapto-4-[2-(trifluoromethyl)phenyl]-1,2,4-triazole (0.78 g) was reacted with 0.63 g of 2-bromo-5-nitrothiazole as in Example 5. Crystallization from ethanol and water gave 0.3 g of 3-hydroxy-5-[(5-nitrothiazol-2-yl)mercapto]-4-[2-(trifluoromethyl)phenyl]-1,2,4-triazole, a yellow solid, MP 183°-185° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05883110
Source datasetuspto-grants-1999_03
ORD IDord-beed3be1ba144001971ab6f0b7c0e89e
Source noteuspto-grants-1999_03