HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(2-Methylpiperidin-1-YL)-3-(trifluoromethyl)benzoic acid → HCID 67529791, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(2-Methylpiperidin-1-YL)-3-(trifluoromethyl)benzoic acid | HCID 59495655 | — |
| Reactant | Tert-butyl {4-[amino(hydroxyimino)methyl]-2-fluorophenoxy}acetate | HCID 72307490 | — |
| Product | HCID 67529791 | HCID 67529791 | — |
Reaction Steps
The title compound was prepared following procedure described for example 4, step 1, but starting from Intermediate 49 (142.14 mg; 0.50 mmol) and Intermediate 15 (172.37 mg; 0.60 mmol). The reaction mixture was filtered through a SPE NH2 column (2 g) and rinsed with ACN. The filtrate was passed through a SPE SCX column (2 g) and rinsed with ACN. After evaporation of the solvents, the crude product was purified by flash chromatography (c-hex/EtOAc: 9.5/0.5), affording the title compound as a white solid. LC/MS (Method B): 536.4 (M+H)+. HPLC (Method A) Rt 7.2 min (Purity: 99.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08202865B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-4f3c505b3c47498b8875b7357d255eb1 |
| Source note | uspto-grants-2012_06 |