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HRID 1268855作成日:2026年10月25日

Potassium Carbonate → 4-Amino-2-(2,2-dioxo-2,3,3a,7a-tetrahydro-1H-2lambda6-benzo[c]thiophen-5-yl)-thieno[3,2-c]pyridine-7-carboxylic acid amide

https://huagongshe.com/reaction/1268855

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物5-Bromo-1,3-dihydro-benzo(c)thiophene 2,2-dioxideHCID 288396—
反応物Potassium AcetateHCID 517044—
反応物Bis(pinacolato)diboraneHCID 2733548—
反応物4-Amino-2-Bromothieno[3,2-C]pyridine-7-CarboxamideHCID 58840713—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
生成物4-Amino-2-(2,2-dioxo-2,3,3a,7a-tetrahydro-1H-2lambda6-benzo[c]thiophen-5-yl)-thieno[3,2-c]pyridine-7-carboxylic acid amideHCID 69065886—

反応条件

温度85 °C

反応手順

To a stirred solution 5-bromo-1,3-dihydro-benzo[c]thiophene 2,2-dioxide (160 mg, 0.65 mmol) 67 (Salor, Milwaukee, Wis.) in DMSO (1 mL) was added bis(pinacolato)diboron (178 mg, 0.70 mmol), KOAc (159 mg, 1.6 mmol) and Pd(dppf)Cl2 DCM complex (22 mg, 0.027 mmol). The mixture was degassed with N2 and heated at 85° C. for 2 h then DMSO (2 mL), H2O (0.5 mL), K2CO3 (223 mg, 1.6 mmol) and 4-amino-2-bromo-thieno[3,2-c]pyridine-7-carboxylic acid amide H2SO4 salt 17 (200 mg, 0.54 mmol) were added. The mixture was stirred at 85° C. for a further 12 h then filtered. The residue was washed with DMSO (2 mL) and the filtrate purified by reverse phase preparative HPLC to yield 68 as a white solid. 1H-NMR (400 MHz, d6-DMSO) δ 8.31 (s, 1H), 8.24 (s, 1H), 8.19 (bs, 1H), 7.97–7.92 (m, 3H), 7.85 (d, 1H), 4.78 (s, 2H), 4.71 (s, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07199119B2
出典データセットuspto-grants-2007_04
ORD IDord-6413c8b5201b434daf564432eb617312
出典メモuspto-grants-2007_04