HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → HCID 57823927, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 4-Fluorophenol | HCID 9732 | — |
| Reactant | HCID 57823936 | HCID 57823936 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Product | HCID 57823927 | HCID 57823927 | — |
Reaction Steps
I-86 is prepared analogously except the starting material was 6-acetyl-5-cyclopropyl-2-(4-phenoxy-phenyl)-benzofuran-3-carboxylic acid methylamide. I-103 and I-104 can be prepared from A-2c by introduction of the p-fluorophenyl by Suzuki coupling with p-fluoro-phenol (see step 5 of example 3), Freidel-Crafts acylation, hydrolysis of the ethyl ester and coupling with methylamine and addition of methyl magnesium bromide as carried described in the current example.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08071797B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-3a3e143136074aae877bc849e7ddb668 |
| Source note | uspto-grants-2011_12 |