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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035187Generated: October 27, 2026

Ethyl 5-(4-methoxyphenyl)-1,3,4-oxadiazole-2-carboxylate → 1-{-4-[(1-{[5-(4-Methoxyphenyl)-1,3,4-oxadiazol-2-yl]carbonyl}azetidin-3-yl)oxy]-2-methylphenyl}-N,N-dimethylmethanamine

https://huagongshe.com/reaction/1035187

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 5-(4-methoxyphenyl)-1,3,4-oxadiazole-2-carboxylateHCID 13407471—
Reactant1-(4-(Azetidin-3-yloxy)-2-methylphenyl)-N,N-dimethylmethanamineHCID 66656350—
Product1-{-4-[(1-{[5-(4-Methoxyphenyl)-1,3,4-oxadiazol-2-yl]carbonyl}azetidin-3-yl)oxy]-2-methylphenyl}-N,N-dimethylmethanamineHCID 5659785174.6%

Reaction Steps

Using a similar protocol as described in Example 16 employing 20C (0.16 g, 0.73 mmol) and ethyl 5-(4-methoxyphenyl)-1,3,4-oxadiazole-2-carboxylate (0.20 g, 0.80 mmol) as starting materials afforded 0.23 g (74%) of 20 as a solid. 1H NMR (600 MHz, CDCl3): δ 2.21 (s, 6H), 2.33 (s, 3H), 3.30 (s, 2H), 3.87 (s, 3H), 4.27-4.35 (m, 1H), 4.58-4.66 (m, 1H), 4.69-4.76 (m, 1H), 5.00-5.15 (m, 2H), 6.53 (d, 1H), 6.58 (s, 1H), 7.00 (d, 2H), 7.14 (d, 1H), 8.08 (d, 2H), MS (APCI+) m/z 423 [M+H]+, LC purity: 98%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546375B2
Source datasetuspto-grants-2013_10
ORD IDord-b299493243444089881fa09046faba4f
Source noteuspto-grants-2013_10