HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl chloroformate → HCID 178526847, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 2-Bromo-5-nitrothiazole | HCID 18211 | — |
| Reactant | 3-Amino-1-(2-(trifluoromethyl)phenyl)thiourea | HCID 723187 | — |
| Reactant | 2-(Trifluoromethyl)phenyl isothiocyanate | HCID 737162 | — |
| Reactant | HCID 178518949 | HCID 178518949 | — |
| Product | HCID 178526847 | HCID 178526847 | 25.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05883110 |
| Source dataset | uspto-grants-1999_03 |
| ORD ID | ord-beed3be1ba144001971ab6f0b7c0e89e |
| Source note | uspto-grants-1999_03 |