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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605646Generated: October 30, 2026

Methyl 6-(2-(7-phenylheptanoyl)oxazol-5-yl)picolinate → 6-[2-(7-Phenylheptanoyl)-1,3-oxazol-5-yl]pyridine-2-carboxylic acid

https://huagongshe.com/reaction/605646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 6-(2-(7-phenylheptanoyl)oxazol-5-yl)picolinateHCID 16110656—
SolventEthyl acetate acetateHCID 22609514—
Product6-[2-(7-Phenylheptanoyl)-1,3-oxazol-5-yl]pyridine-2-carboxylic acidHCID 1611071557%

Reaction Steps

The title compound was prepared from methyl 6-(2-(7-phenylheptanoyl)oxazol-5-yl)picolinate (9 mg, 0.059 mmol) following General Procedure E. Preparative thin layer chromatography (2% AcOH/EtOAc) yielded the title compound as a white solid (5 mg, 57%): 1H NMR (THF-d8, 500 MHz) δ 8.11-8.04 (m, 4H), 7.22-7.08 (m, 5H), 3.08 (t, 2H, J=7.5 Hz), 2.61 (t, 2H, J=7.5 Hz), 1.76-1.68 (m, 2H), 1.68-1.62 (m, 2H), 1.45-1.41 (m, 4H); 13C NMR (THF-d8, 125 MHz) δ 185.6, 163.1, 156.4, 151.4, 147.6, 144.7, 141.0, 137.1, 126.7, 126.5, 126.1, 123.9, 122.8, 121.1, 37.1, 34.3, 30.0, 27.6, 27.5, 22.2; MALDI-FTMS m/z 379.1645 (M+H+, C22H23N2O4, requires 379.1652).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915270B2
Source datasetuspto-grants-2011_03
ORD IDord-7509b9214d054acea8002bb6fe77dea7
Source noteuspto-grants-2011_03