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HRID 501049作成日:2026年10月23日

Benzo(B)Thiophene-2-Boronic Acid → 5-(1-Benzothien-2-yl)pyridine-2-carboxamide

https://huagongshe.com/ja/reaction/501049

反応式

関与物質

役割名称HCID仕込み量
反応物Benzo(B)Thiophene-2-Boronic AcidHCID 2359—
反応物Potassium CarbonateHCID 11430—
反応物5-Bromopyridine-2-carboxamideHCID 735151—
触媒Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
溶媒DimethylformamideHCID 6228—
生成物5-(1-Benzothien-2-yl)pyridine-2-carboxamideHCID 250149303.6%

反応手順

2-Benzothienylboronic acid (1.8 mmol), 5-bromopyridine-2-carboxamide (1.2 mmol), 2M K2CO3 (2.4 mL), Pd(dppf)Cl2 (0.12 mmol) were mixed and stirred at 80° C. in DMF for 3 h. The reaction mixture was filtered and to the filtrated was added EtOAc and H2O. The layers were separated and the aqueous phase was extracted twice with EtOAc. The organic extracts were dried over Na2SO4. The solvent was evaporated in vacuo to give a brown solid. The crude was subjected to reverse phase HPLC to afford the title compound as a light brown solid (11 mg). 1H NMR δ ppm 9.07 (d, 1 H) 8.34 (dd, 1 H) 8.24-8.02 (m, 5 H) 7.73 (s br, 1 H) 7.54-7.37 (m, 2 H); MS m/z 255 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07772256B2
出典データセットuspto-grants-2010_08
ORD IDord-a032e3afb19e418595dd11b2e977e424
出典メモuspto-grants-2010_08