HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446910Generated: October 25, 2026
Dicyclohexylcarbodiimide → HCID 86642295, compound
https://huagongshe.com/reaction/446910
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 3-Chlorophenyl isothiocyanate | HCID 75449 | — |
| Reactant | HCID 178462184 | HCID 178462184 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 86642295 | HCID 86642295 | 48.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481538B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-99b478e2c89843c2a1f93812d9885667 |
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| Source note | uspto-grants-2013_07 |
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