HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 14851921, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | HCID 14851918 | HCID 14851918 | — |
| Reactant | HCID 14894666 | HCID 14894666 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 14851921 | HCID 14851921 | — |
Reaction Steps
The title compound was obtained by reacting rac-6-(2-fluorophenyl)-4-hydroxy-8-iodo-1-methyl-4H-[1,2,4]triazolo[4,3-a][4,1]benzodiazepine with 3,4-dihydro-1(2-propynyl)-2(1H)-quinolinone under the conditions used in Example 37. The product was isolated by chromatography over the 50-fold amount of silica gel using 5% (v/v) of ethanol in methylene chloride. The combined good fractions were evaporated and the residue was crystallized from methanol/ethyl acetate to give colorless crystals of rac-1-{3-[6-(2-fluorophenyl)-4-hydroxy-1-methyl-4H-[1,2,4]triazolo[4,3-a][4,1]benzodiazepin-8-yl]-2-propynyl}-3,4-dihydro-2(1H)-quinolinone with m.p. 253°-255° with decomposition. These crystals contained molar equivalents of water.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04959361 |
| Source dataset | uspto-grants-1990_09 |
| ORD ID | ord-b9e57996449a4965b0ae3a6782a1f32b |
| Source note | uspto-grants-1990_09 |