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HRID 1943139作成日:2026年10月26日

Sodium Iodide → HCID 58001733、化合物

https://huagongshe.com/reaction/1943139

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物TriethylamineHCID 8471—
反応物Methanesulfonic anhydrideHCID 81560—
反応物1,1-Dimethylethyl (1-{2-hydroxy-3-[7-(methyloxy)-2-oxo-3,4-dihydro-1,8-naphthyridin-1(2H)-yl]propyl}-4-piperidinyl)carbamateHCID 69046556—
溶媒ChloroformHCID 6212—
生成物HCID 58001733HCID 5800173370%

反応条件

温度80 °C

反応手順

A solution of 1,1-dimethylethyl (1-{2-hydroxy-3-[7-(methyloxy)-2-oxo-3,4-dihydro-1,8-naphthyridin-1(2H)-yl]propyl}-4-piperidinyl)carbamate (301 mg, 0.694 mmol) in chloroform (10 ml) and triethylamine (0.24 ml, 1.735 mmol) at rt under argon was treated with methanesulfonic anhydride (242 mg, 1.388 mmol) and heated at reflux for 2 h. The reaction mixture was then evaporated and dissolved in acetonitrile (10 ml), treated with sodium iodide (520 mg, 3.47 mmol) and heated at 80° C. for 0.25 h. The mixture was then cooled, evaporated was then treated with water (200 ml), extracted with 20% methanol/DCM (3×200 ml). The organic extracts were dried (MgSO4), evaporated and chromatographed (0-10% methanol/DCM) to give the product as an orange oil (194 mg, 70%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08389524B2
出典データセットuspto-grants-2013_03
ORD IDord-adbb2472c7e248c0baf58c5aff52064a
出典メモuspto-grants-2013_03