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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219929Generated: October 26, 2026

4-(2-Methylpiperidin-1-YL)-3-(trifluoromethyl)benzoic acid → HCID 67529791, compound

https://huagongshe.com/reaction/219929

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-Methylpiperidin-1-YL)-3-(trifluoromethyl)benzoic acidHCID 59495655—
ReactantTert-butyl {4-[amino(hydroxyimino)methyl]-2-fluorophenoxy}acetateHCID 72307490—
ProductHCID 67529791HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202865B2
Source datasetuspto-grants-2012_06
ORD IDord-4f3c505b3c47498b8875b7357d255eb1
Source noteuspto-grants-2012_06