HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Fluorophenol → HCID 66874849, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Fluorophenol | HCID 9743 | — |
| Reactant | 1-Nonanol, 9-bromo- | HCID 108700 | — |
| Reactant | (R)-benzyl 3-amino-4-(dimethylamino)butanoate dihydrochloride | HCID 46223507 | — |
| Reactant | HCID 66874069 | HCID 66874069 | — |
| Reactant | HCID 66875184 | HCID 66875184 | — |
| Product | HCID 66874849 | HCID 66874849 | — |
Reaction Steps
The title compound, m/e=397.4 ([M+H]+), was produced in analogy with example 18, steps 1 to 4. Thus, 3-fluorophenol was alkylated in step 1 with 9-bromo-1-nonanol, leading to 9-(3-fluoro-phenoxy)-nonan-1-ol, which was oxidized in step 2 to 9-(3-fluoro-phenoxy)-nonanoic acid. This was coupled in step 3 with (R)-3-amino-4-dimethylamino-butyric acid benzyl ester dihydrochloride to produce (R)-4-dimethylamino-3-[9-(3-fluoro-phenoxy)-nonanoylamino]-butyric acid benzyl ester, which was hydrogenated in step 4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08344027B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-2050993a7b3e457d87b8b22bd70311cb |
| Source note | uspto-grants-2013_01 |