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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1268855생성일: 2026년 10월 26일

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

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물5-Bromo-1,3-dihydro-benzo(c)thiophene 2,2-dioxideHCID 288396—
반응물Potassium AcetateHCID 517044—
반응물Bis(pinacolato)diboraneHCID 2733548—
반응물4-Amino-2-Bromothieno[3,2-C]pyridine-7-CarboxamideHCID 58840713—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물4-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—

반응 조건

온도85 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07199119B2
출처 데이터셋uspto-grants-2007_04
ORD IDord-6413c8b5201b434daf564432eb617312
출처 메모uspto-grants-2007_04