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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446910Generated: October 25, 2026

Dicyclohexylcarbodiimide → HCID 86642295, compound

https://huagongshe.com/reaction/446910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant3-Chlorophenyl isothiocyanateHCID 75449—
ReactantHCID 178462184HCID 178462184—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
ProductHCID 86642295HCID 8664229548.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

(Step 8-ii) A mixture of (R)-benzyl 1-(5-mercapto-4-amino-4H-1,2,4-triazol-3-yl)ethylcarbamate (1.32 g, 4.5 mmol) in ethanol (15 mL) was heated to 80° C. and 3-chlorophenylisothiocyanate (1.3 g, 7.65 mmol) and dicyclohexylcarbodiimide (1.11 g, 5.4 mmol) were added. After 4 hours, the reaction was cooled, diluted with an equal volume of ether, and filtered. The filter cake was washed with additional ether and the collected solids dried in vacuo to provide 0.94 g of (R)-benzyl 1-(6-(3-chlorophenylamino)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-3-yl)ethylcarbamate: ESMS MH+=429.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481538B2
Source datasetuspto-grants-2013_07
ORD IDord-99b478e2c89843c2a1f93812d9885667
Source noteuspto-grants-2013_07