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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173075Generated: November 1, 2026

Pentylamine → pentyl[2'-(1-trityl-1H-tetrazol-5-yl)biphenyl-4-ylmethyl]amine

https://huagongshe.com/reaction/1173075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPentylamineHCID 8060—
ReactantPotassium CarbonateHCID 11430—
Reactant5-(4'-(Bromomethyl)(1,1'-biphenyl)-2-yl)-1-trityl-1H-tetraazoleHCID 10053461—
SolventTetrahydrofuranHCID 8028—
Productpentyl[2'-(1-trityl-1H-tetrazol-5-yl)biphenyl-4-ylmethyl]amineHCID 19024425—

Reaction Steps

A solution of 5-(4′-bromomethylbiphenyl-2-yl)-1-trityl-1H-tetrazole (30 g, 50 mmol), n-amylamine (45 ml, 650 mmol) and potassium carbonate (7.5 g, 50 mmol) in THF (45 mL) were stirred overnight at room temperature. The mixture was concentrated in vacuo, and then extracted with 1M aq. KOH (50 mL) and chloroform (3×200 mL). The combined organic fractions were dried over Na2SO4, filtered and concentrated in vacuo to yield crude pentyl[2′-(1-trityl-1H-tetrazol-5-yl)biphenyl-4-ylmethyl]amine, which was used without further purification. A solution of the crude material (30 g) in 4M HCl in 1,4-dioxane (300 mL) was stirred at room temperature. After 1 hour, the precipitate was filtered and washed with hexane to afford the title compound as the HCl salt (18.0 g). MS m/z: [M+H]+ calcd for C19H23N5, 321.20. found 322.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834041B2
Source datasetuspto-grants-2010_11
ORD IDord-8d9bd7f9eb1b4146aa24d19b9d2b7cb7
Source noteuspto-grants-2010_11