HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 14851929, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | HCID 14851914 | HCID 14851914 | — |
| Reactant | HCID 14894694 | HCID 14894694 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 14851929 | HCID 14851929 | — |
Reaction Steps
This compound was prepared by reacting rac-4-(2-chloro-phenyl)-2-iodo-6,9-dimethyl-6H-thieno-[3,2-f][1,2,4]triazolo[4,3a][4,1]diazepine (from example 108) with 5-(2-propynyl)-6(5H) phenanthridinone under the conditions described 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 product was crystallized from ethanol to give yellowish crystals of the title compound with mp, 182°-186° with foaming. These crystals contained according to analytical data molar amounts of water.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04959361 |
| Source dataset | uspto-grants-1990_09 |
| ORD ID | ord-e7118b68d22444738543706958045fcf |
| Source note | uspto-grants-1990_09 |