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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375251Generated: October 27, 2026

1,3-Dimethylamylamine → N-(1,3-dimethylpentyl)-2'-methyl-5'-(5-methyl-1,3,4-oxadiazol-2-yl)-1,1'-biphenyl-4-carboxamide

https://huagongshe.com/reaction/1375251

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DimethylamylamineHCID 7753—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 21078800HCID 21078800—
SolventDimethylformamideHCID 6228—
ProductN-(1,3-dimethylpentyl)-2'-methyl-5'-(5-methyl-1,3,4-oxadiazol-2-yl)-1,1'-biphenyl-4-carboxamideHCID 21078780—

Reaction Steps

2′-Methyl-5′-(5-methyl-1,3,1-oxadiazol-2-yl)-1,1′-biphenyl-4-carboxylic acid (11.3 mg, 0.034 mmol), HOBT (6.0 mg, 0.044 mmol), 1-(3-dimethylaminopropyl)-3-ethyl carbodiimide hydrochloride (8.0 mg, 0.042 mmol) and 1,3-dimethylpentylamine (0.34 mmol) were mixed in DMF (0.7 ml) and the reaction left at room temperature for 18 h. The DMF was evaporated under vacuum and the residue partitioned between DCM (0.4 ml) and water (0.4 ml). The organic phase was washed with aqueous sodium hydroxide (0.5M, 0.2 ml) and the DCM evaporated under vacuum. The residue was purified by mass directed HPLC to give N-(1,3-dimethylpentyl)-2′-methyl-5′-(5-methyl-1,3,4-oxadiazol-2-yl)-1,1′-biphenyl-4-carboxamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07166623B2
Source datasetuspto-grants-2007_01
ORD IDord-f7b864bfbc1e4e2baf59e6cde6838814
Source noteuspto-grants-2007_01