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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131696Generated: October 31, 2026

Methyl iodide → 2'-Methyl-N-methyl-5'-(5-methyl-1,3,4-oxadiazol-2-yl)-N-(4-phenoxybenzyl)-1,1'-biphenyl-4-carboxamide

https://huagongshe.com/reaction/131696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant2'-methyl-5'-(5-methyl-1,3,4-oxadiazol-2-yl)-N-(4-phenoxybenzyl)-1,1'-biphenyl-4-carboxamideHCID 10116392—
Product2'-Methyl-N-methyl-5'-(5-methyl-1,3,4-oxadiazol-2-yl)-N-(4-phenoxybenzyl)-1,1'-biphenyl-4-carboxamideHCID 10278034—

Reaction Steps

2′-Methyl-N-methyl-5′-(5-methyl-1,3,4-oxadiazol-2-yl)-N-(4-phenoxybenzyl)-1,1′-biphenyl-4-carboxamide was prepared from 2′-methyl-5′-(5-methyl-1,3,4-oxadiazol-2-yl)-N-(4-phenoxybenzyl)-1,1′-biphenyl-4-carboxamide and iodomethane using method L. NMR; δH [2H6]—DMSO 7.89,(1H, d), 7.76,(1H, s), 7.55-7.48,(5H, m), 7.40-7.36,(3H, m), 7.23,(1H, b), 7.13,(1H, t), 7.01,(4H, m), 4.684.52,(2H, m), 2.91,(3H, s), 2.55,(3H, s), 2.32,(3H, s). LCMS; retention time 3.85 min, MH+ 490.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384963B2
Source datasetuspto-grants-2008_06
ORD IDord-af98839b0f7b4bfeb7771f901697a241
Source noteuspto-grants-2008_06