HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 18433429, compound → HCID 22728127, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 18433429 | HCID 18433429 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 22728127 | HCID 22728127 | — |
Reaction Steps
5-(4-Amino-2,6-dimethyl-phenoxy)-N-cyclobutyl-2-hydroxy-N-methyl-benzamide was prepared from N-cyclobutyl-5-(2,6-dimethyl-4-nitro-phenoxy)-2-hydroxy-N-methyl-benzamide according to a procedure analogous to that described in EXAMPLE 4, Step A. Methanol was used instead of ethanol as a co-solvent. The reaction mixture was hydrogenated for 2 hours. Then, the mixture was filtered through Celite® and concentrated, and the title product of Step F was used in the next step without purification. MS (APCI+) Calc.: 340.4, Found: 341.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06441015B2 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-d9167513394c4845b2b4b21a3425aed0 |
| Source note | uspto-grants-2002_08 |