戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 272053作成日:2026年10月26日

Sodium Thiosulfate → Methyl 3-amino-6-iodopyrazine-2-carboxylate

https://huagongshe.com/reaction/272053

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium ThiosulfateHCID 24477—
反応物Methyl 3-aminopyrazinecarboxylateHCID 72669—
反応物N-IodosuccinimideHCID 120273—
溶媒DimethylformamideHCID 6228—
生成物Methyl 3-amino-6-iodopyrazine-2-carboxylateHCID 1108712461.5%

反応条件

温度70 °C

反応手順

Methyl 3-amino-2-pyrazinecarboxylate (10 g, 65.3 mmol) and N-iodosuccinimide (24 g, 106.7 mmol) were dissolved in anhydrous DMF (150 mL) and the mixture was stirred at 70° C. for 15 hours under a nitrogen atmosphere. The mixture was then cooled to room temperature and a saturated aqueous solution of sodium thiosulfate (400 mL) was added. The suspension was sonicated for 15 minutes, concentrated under vacuum and dispersed in water. The crude product was filtered off and washed with cold ethanol. The residue was crystallized from ethanol, using decolorizing charcoal to afford 3-amino-6-iodo-pyrazine-2-carboxylic acid methyl ester (11.2 g, 61% yield) as orange needles. 1H-NMR (d6-DMSO) δ: 8.57 [1H] s, 7.59 [2H] s,br, 3.93 [3H] s. MS: m/z 280 [MH+].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07452993B2
出典データセットuspto-grants-2008_11
ORD IDord-57810c7f678345f98e9ba23883ec6ff3
出典メモuspto-grants-2008_11