HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formic Acid → HCID 18399233, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 18398907 | HCID 18398907 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 18399233 | HCID 18399233 | — |
Reaction Steps
To formic acid (3 ml) is added acetic anhydride (3 ml), and the mixture is stirred at room temperature for four hours. To the reaction mixture is added the compound obtained in Example 176 (500 mg), and the mixture is stirred at room temperature overnight. The mixture is further stirred at 60° C. overnight. After the reaction is complete, to the reaction mixture are added water and ethyl acetate. The ethyl acetate layer is separated, washed with water, dried, and concentrated under reduced pressure. The residue is purified by silica gel column chromatography (solvent; chloroform:acetone=10:1) to give 6,7-dimethoxy-2-[3-(formylamino)phenyl]-4-(3-bromo-4,5-dimethoxyphenyl)-3-methoxycarbonyl-1(2H)-isoquinolinone as listed in Table 16.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06486155B1 |
| Source dataset | uspto-grants-2002_11 |
| ORD ID | ord-5b7a0ba175774f03850e08ea6d2b92df |
| Source note | uspto-grants-2002_11 |