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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605666Generated: October 30, 2026

Methyl 5-(2-(7-phenylheptanoyl)oxazol-5-yl)thiophene-2-carboxylate → HCID 16110661, compound

https://huagongshe.com/reaction/605666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 5-(2-(7-phenylheptanoyl)oxazol-5-yl)thiophene-2-carboxylateHCID 16110718—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 16110661HCID 1611066143.5%

Reaction Steps

The title compound was prepared from methyl 5-(2-(7-phenylheptanoyl)oxazol-5-yl)thiophene-2-carboxylate (7 mg, 0.018 mmol) following General Procedure E. Preparative thin layer chromatography (10% MeOH/CH2Cl2) yielded the title compound as a white solid (3 mg, 41%): 1H NMR (THF-d8, 500 MHz) δ 7.73 (d, 1H, J=3.5 Hz), 7.72 (s, 1H), 7.55 (d, 1H, J=4.0 Hz), 7.22-7.08 (m, 5H), 3.03 (t, 2H, J=7.0 Hz), 2.60 (t, 2H, J=7.5 Hz), 1.73-1.71 (m, 2H), 1.65-1.61 (m, 2H), 1.42-1.40 (m, 4H); 13C NMR NMR (THF-d8, 125 MHz) δ 185.1, 164.0, 155.8, 147.0, 141.0, 134.8, 132.7, 132.1, 126.7, 126.5, 124.9, 123.9, 123.3, 37.0, 34.3, 30.0, 27.6, 27.5, 22.2; MALDI-FTMS m/z 384.1272 (M+H+, C21H22NO4S, requires 384.1264).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915270B2
Source datasetuspto-grants-2011_03
ORD IDord-f58c7de764fb42c6a7e9ac317f72b846
Source noteuspto-grants-2011_03