Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1423215Generated: November 3, 2026

Methyl 2-(3-methyl-1,2,4-oxadiazol-5-yl)acetate → (S)-1-(2-benzyl-4-(3-cyclobutoxy-4-methoxyphenyl)piperazin-1-yl)-2-(3-methyl-1,2,4-oxadiazol-5-yl)ethanone

https://huagongshe.com/reaction/1423215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-(3-methyl-1,2,4-oxadiazol-5-yl)acetateHCID 54453761—
ReactantHCID 58188985HCID 58188985—
Product(S)-1-(2-benzyl-4-(3-cyclobutoxy-4-methoxyphenyl)piperazin-1-yl)-2-(3-methyl-1,2,4-oxadiazol-5-yl)ethanoneHCID 5818899735%

Reaction Steps

Prepared using the same procedure described in Example 275 from (S)-3-benzyl-1-(3-cyclobutyloxy-4-methoxy-phenyl)-piperazine and (3-methyl-[1,2,4]oxadiazol-5-yl)-acetic acid methyl ester with heating for 5 days to afford the title compound as an off-white solid (49 mg, 35%). LC/MS (Method B) 3.80 min, [M+1]+ 477.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927546B2
Source datasetuspto-grants-2015_01
ORD IDord-11837709ee7e44a583297f9a7954ddab
Source noteuspto-grants-2015_01