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HRID 709310作成日:2026年10月27日

3-Iodophenol → (E)-tert-butyl 4-(4-(5-(3-hydroxystyryl)pyrazin-2-ylamino)phenylsulfonyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/709310

反応式

関与物質

役割名称HCID仕込み量
反応物3-IodophenolHCID 12272—
反応物Phosphine, tris(4-methylphenyl)-HCID 13956—
反応物DiisopropylethylamineHCID 81531—
反応物Tert-butyl 4-(4-(5-vinylpyrazin-2-ylamino)phenylsulfonyl)piperazine-1-carboxylateHCID 67324584—
触媒palladium(II) acetateHCID 167845—
溶媒DimethylformamideHCID 6228—
生成物(E)-tert-butyl 4-(4-(5-(3-hydroxystyryl)pyrazin-2-ylamino)phenylsulfonyl)piperazine-1-carboxylateHCID 6732568878.5%

反応条件

温度120 °C

反応手順

A mixture of tert-butyl 4-(4-(5-vinylpyrazin-2-ylamino)phenylsulfonyl)piperazine-1-carboxylate (40 mg, 0.09 mmol), 3-iodophenol (19 mg, 0.09 mmol), Pd(OAc)2 (1.2 mg, 0.005 mmol), tri-p-tolylphosphine (2.5 mg, 0.008 mmol), and DIEA (31 μL, 0.18 mmol) in DMF (3 ml) was heated at 120° C. for 18 h after which, it was filtered with a pad of celite and partitioned between ethyl acetate and water. The organic layer was separated and the aqueous layer was extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over MgSO4, celite filtered and concentrated under reduced pressure. The crude product was purified by flash chromatography using (20% to 40% Ethyl acetate/Hexane) as a solvent to afford title compound (38 mg, 78% yield). MS m/z: 538 [M+1].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09180127B2
出典データセットuspto-grants-2015_11
ORD IDord-4c6951e557ba4a1cb8027db3defda424
出典メモuspto-grants-2015_11