HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 14071251, compound → HCID 9894694, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 14071251 | HCID 14071251 | — |
| Reactant | HCID 21937476 | HCID 21937476 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 9894694 | HCID 9894694 | — |
Reaction Steps
A mixture containing 2-trifluoromethylbenzylisothiocyanate (1 g, 0.0046 mol) and 6-(2-chlorophenyl)-7,8,9,10-tetrahydro-1-methyl-4H-pyrido[4′,3′;4,5]thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine (1.22 g, 0.0033 mol) in 20 ml of dichloromethane is agitated at a temperature close to 20° C. for 1 hour. The reaction mixture is evaporated to dryness. 40 ml of ethyl acetate is added to the residual oil. After separation of the insoluble part, the solvent is evaporated off. 40 ml of isopropyl ether is added until precipitation of the product then filtration on frit and washing with isopropyl ether. The solid obtained (1.2 g, 63%) is dried and a beige powder is obtained. Melting point: 178–184° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07015213B1 |
| Source dataset | uspto-grants-2006_03 |
| ORD ID | ord-0bf259698d8e48ce847cefc814798707 |
| Source note | uspto-grants-2006_03 |