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HRID 9920作成日:2026年10月26日

2-(2-hydroxy-ethyl-amino)-6-(4-benzyloxycarbonylamino-phenyl-amino)-9-ethyl-9H-purine → 6-(4-amino-phenyl-amino)-9-ethyl-2-(2-hydroxy-ethyl-amino)-9H-purine

https://huagongshe.com/reaction/9920

反応式

関与物質

役割名称HCID仕込み量
反応物2-(2-hydroxy-ethyl-amino)-6-(4-benzyloxycarbonylamino-phenyl-amino)-9-ethyl-9H-purineHCID 21988243—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物6-(4-amino-phenyl-amino)-9-ethyl-2-(2-hydroxy-ethyl-amino)-9H-purineHCID 21988284—

反応手順

0.45 g (1 mmol) of 2-(2-hydroxy-ethyl-amino)-6-(4-benzyloxycarbonylamino-phenyl-amino)-9-ethyl-9H-purine (prepared according to Example 107) are hydrogenated with 0.1 g of 10% Pd/C in 8 ml of methanol at RT for 5 h. The catalyst is filtered off, the residue on the filter is rinsed with dioxane/water (95:5) and the solvent is removed in vacuo. The desired compound, 6-(4-amino-phenyl-amino)-9-ethyl-2-(2-hydroxy-ethyl-amino)-9H-purine, can be isolated in crystalline form by this procedure; m.p. 210° C.; FAB-MS: (M+H)+=314; Rf=0.15 (methylene chloride:methanol=9:1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091346B1
出典データセットuspto-grants-2006_08
ORD IDord-070bedf9f90b4842b0782e22b1a25f04
出典メモuspto-grants-2006_08