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HRID 386145作成日:2026年10月25日

Tetrabutylammonium Fluoride → 5-(1-Methyl-1H-1,2,3-triazol-4-yl)-2-{[6-(morpholin-4-ylmethyl)pyridin-2-yl]amino}thiophene-3-carboxamide

https://huagongshe.com/reaction/386145

反応式

関与物質

役割名称HCID仕込み量
反応物Tetrabutylammonium FluorideHCID 2724141—
反応物2-{[6-(Morpholin-4-ylmethyl)pyridin-2-yl]amino}-5-{1-[(trimethylsilyl)methyl]-1H-1,2,3-triazol-4-yl}thiophene-3-carboxamideHCID 59525568—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物5-(1-Methyl-1H-1,2,3-triazol-4-yl)-2-{[6-(morpholin-4-ylmethyl)pyridin-2-yl]amino}thiophene-3-carboxamideHCID 59525702—

反応手順

To a solution of 2-{[6-(morpholin-4-ylmethyl)pyridin-2-yl]amino}-5-{1-[(trimethylsilyl)methyl]-1H-1,2,3-triazol-4-yl}thiophene-3-carboxamide (65 mg, 0.14 mmol) in THF (2.0 mL) was added TBAF (1.0 M in THF, 0.276 ml, 0.276 mmol). The reaction was stirred at room temperature for 4 h. The solution was diluted with water and extracted with 5:1 CH2Cl2:MeOH (3×). The combined organic layers were dried (MgSO4), filtered, and evaporated. The crude solid was triturated with CH2Cl2 and filtered to isolate the title compound as a colorless solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08367706B2
出典データセットuspto-grants-2013_02
ORD IDord-b5cec79b66c3402f93cfa6f31eec522e
出典メモuspto-grants-2013_02