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HRID 32016作成日:2026年10月24日

Sodium Thiosulfate Pentahydrate → 1-[6-(4-Bromo-2-chloro-phenylamino)-7-fluoro-3H-benzoimidazol-5-yl]-2-ethoxy-ethanone

https://huagongshe.com/ja/reaction/32016

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium Thiosulfate PentahydrateHCID 61475—
反応物Sodium BicarbonateHCID 516892—
反応物1-[6-(4-Bromo-2-chloro-phenylamino)-7-fluoro-3H-benzoimidazol-5-yl]-2-ethoxy-ethanolHCID 21114164—
生成物1-[6-(4-Bromo-2-chloro-phenylamino)-7-fluoro-3H-benzoimidazol-5-yl]-2-ethoxy-ethanoneHCID 21114165—

反応手順

The title compound is prepared from 1-[6-(4-bromo-2-chloro-phenylamino)-7-fluoro-3H-benzoimidazol-5-yl]-2-ethoxy-ethanol 10o according to the procedure described in Example 42, Step B except that the reaction mixture is not treated with saturated aqueous NaHCO3 containing sodium thiosulfate pentahydrate. MS APCI (+) m/z 426, 428 (M+, Br pattern) detected; 1H NMR (400 MHz, CD3OD) δ 8.36 (s, 1H), 8.04 (s, 1H), 7.51 (d, 1H), 7.21 (dd, 1H), 6.51 (dd, 1H), 4.76 (s, 2H), 3.57 (q, 2H), 1.19 (t, 3H); 19F NMR (376 MHz, CD3OD) −133.96 (s).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07425637B2
出典データセットuspto-grants-2008_09
ORD IDord-316be2865f284132a2a1f5d5729f59d8
出典メモuspto-grants-2008_09