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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2043590Generated: November 2, 2026

Benzylamine → HCID 53629116, compound

https://huagongshe.com/reaction/2043590

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantTriethylamineHCID 8471—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
ReactantHCID 57743028HCID 57743028—
SolventDimethylformamideHCID 6228—
ProductHCID 53629116HCID 5362911643%

Reaction Steps

In a 10 ml, three necked flask fitted with a magnetic stirrer, under inert atmosphere, {5-[(2-oxo-4-propylpyrrolidin-1-yl)methyl]-1H-imidazol-1-yl}acetic acid x50 (0.1 g, 0.33 mmol) is dissolved in DMF (1 ml). Triethylamine (0.1 ml, 0.66 mmol), benzylamine (37 μl, 0.33 mmol) and TBTU (0.16 g, 0.33 mmol) are added and the mixture is stirred for 0.5 h at room temperature. An additional amount of benzylamine (0.0165 mmol) is added and stirring is continued overnight. The solvent is evaporated and the residue is purified by chromatography on silicagel (AcOEt/MeOH/NH4OH: 90/9/1 (v/v/v)). The product is treated with a methanolic solution of HCl and the obtained solid is recrystallized from acetonitrile to afford N-benzyl-2-{5-[(2-oxo-4-propylpyrrolidin-1-yl)methyl]-1H-imidazol-1-yl}acetamide 124.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586623B2
Source datasetuspto-grants-2013_11
ORD IDord-fa7fd301c6194088bef7cb3877dec32e
Source noteuspto-grants-2013_11