HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Trifluoromethyl)phenyl isothiocyanate → HCID 9917559, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Trifluoromethyl)phenyl isothiocyanate | HCID 737162 | — |
| Reactant | HCID 9868167 | HCID 9868167 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 9917559 | HCID 9917559 | 24% |
Reaction Steps
Trifluoromethylphenylisothiocyanate (0.56 g, 0.0027 mol) is added to a mixture containing 1-benzyl-6-(2-chlorophenyl)-7,8,9,10-tetrahydro-4H-pyrido[4′,3′;4,5]thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine (0.8 g, 0.0018 mol) in anhydrous 1,2-dichloroethane (13 ml). The reaction medium is agitated at ambient temperature for 12 hours. The precipitate is filtered on frit then washed with isopropyl ether, with ethyl acetate then with isopentane and finally dried under vacuum. 0.28 g (24%) of final product is obtained in the form of a pale yellow coloured solid. Melting point: 239–240° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07015213B1 |
| Source dataset | uspto-grants-2006_03 |
| ORD ID | ord-7869369e6985408c86b77f636382fe6e |
| Source note | uspto-grants-2006_03 |