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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410569Generated: November 2, 2026

3-(Methoxymethyl)-4-(2-methylpiperidin-1-yl)benzoic acid → HCID 66678478, compound

https://huagongshe.com/reaction/2410569

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Methoxymethyl)-4-(2-methylpiperidin-1-yl)benzoic acidHCID 59495804—
ReactantHCID 76685331HCID 76685331—
ProductHCID 66678478HCID 66678478—

Reaction Steps

Tert-butyl 3-[(3-{5-[3-(methoxymethyl)-4-(2-methylpiperidin-1-yl)phenyl]-1,2,4-oxadiazol-3-yl}benzyl)oxy]propanoate was prepared following the general procedure 3 starting from Intermediate 2 and Intermediate 20. It was hydrolyzed following general procedure 8 to afford the title compound as a pale yellow powder. 1H NMR (DMSO-d6, 300 MHz) δ 8.19 (m, 1H), 8.06 (m, 3H), 7.57 (m, 2H), 7.39 (m, 1H), 4.60 (s, 2H), 4.57 (m, 2H), 3.70 (t, J=6.2 Hz, 2H), 3.42 (s, 3H), 3.24 (m, 1H), 3.03 (m, 1H), 2.63 (m, 1H), 2.54 (t, J=6.2 Hz, 2H), 1.85-1.30 (m, 6H), 0.86 (d, J=6.1 Hz, 3H). LC/MS (Method B): 466.4 (M+H)+, 464.4 (M−H)−. HPLC (Method A) Rt 3.30 min (Purity: 98.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815919B2
Source datasetuspto-grants-2014_08
ORD IDord-41915c04522f4560816096848d2f9f67
Source noteuspto-grants-2014_08