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HRID 377012作成日:2026年10月26日

Borane;pyridine → p-NO2-Bn-Cyclen

https://huagongshe.com/reaction/377012

反応式

関与物質

役割名称HCID仕込み量
反応物Borane;pyridineHCID 2723995—
反応物2-(4-Nitrobenzyl)-3,6,9,12-tetraoxo-1,4,7,10-tetraazacyclododecaneHCID 19360715—
溶媒PyridineHCID 1049—
生成物p-NO2-Bn-CyclenHCID 10892179—

反応条件

温度120 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06022966
出典データセットuspto-grants-2000_02
ORD IDord-c56b42dd4f524a2cb77c8c68b9f4c7bc
出典メモuspto-grants-2000_02