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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1457276Generated: October 26, 2026

Borane;pyridine → p-NO2-Bn-Cyclen

https://huagongshe.com/reaction/1457276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBorane;pyridineHCID 2723995—
Reactant2-(4-Nitrobenzyl)-3,6,9,12-tetraoxo-1,4,7,10-tetraazacyclododecaneHCID 19360715—
SolventPyridineHCID 1049—
Productp-NO2-Bn-CyclenHCID 10892179—

Reaction Conditions

Temperature120 °C

Reaction Steps

Borane-pyridine (available from Aldrich) is added to a suspension of 2-(4-nitrobenzyl)-3,6,9,12-tetraoxo-1,4,7,10-tetraazacyclododecane in pyridine. The mixture is heated under reflux at 120° C. for 14 hours. The solvent is removed under reduced pressure. The residue is taken up in methanol and heated under reflux for 2 hours. The solvent is removed under reduced pressure. The residue is dissolved in methanol and re-evaporated. The solid residue is purified by chromatography on reverse phase Baker G18 silica gel available from J. T. Baker, Inc., Phillipsburg, N.J. Conversion of this product to nitro-benzyl-DOTA is accomplished via the procedure discussed in Renn et al., Bioconj. Chem., 3:563-569, 1992 or as set forth is subpart A above.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05847121
Source datasetuspto-grants-1998_12
ORD IDord-b9c5d450c3e248ec8f5aac9e15b1b0d3
Source noteuspto-grants-1998_12