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HRID 984707作成日:2026年10月26日

Formic Acid → 2-Bromo-6-(sulfamoylamino)naphthalene

https://huagongshe.com/reaction/984707

反応式

関与物質

役割名称HCID仕込み量
反応物Formic AcidHCID 284—
反応物Chlorosulfonyl isocyanateHCID 70918—
反応物2-Amino-6-bromonaphthaleneHCID 348404—
溶媒BenzeneHCID 241—
生成物2-Bromo-6-(sulfamoylamino)naphthaleneHCID 22559043—

反応手順

A solution of chlorosulfonyl isocyanate (870 μl, WAKO) in benzene (10 ml) was added dropwise with formic acid (377 μl, WAKO) under ice cooling, warmed to room temperature, stirred for 19.5 hours, then heated to 40° C. and further stirred for 4 hours. The reaction mixture was added dropwise with a solution (5 ml) of 2-amino-6-bromonaphthalene (443 mg) in benzene under ice cooling, warmed to room temperature and stirred for 21.5 hours. The reaction mixture was filtered, and the obtained solid was added with ethyl acetate and mixed. The mixture was filtered again, and then the solvent was evaporated under reduced pressure. The residue was purified by column chromatography (Quad, hexane:ethyl acetate=2:1) to obtain the title compound (Intermediate 28, 158 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06867320B2
出典データセットuspto-grants-2005_03
ORD IDord-a3cb2ca8d20d416a9157656051eb274a
出典メモuspto-grants-2005_03