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

HRID 1868308

Reaktionsgleichung

Reaktionsgleichung von HRID 1868308
Br[C:2]1[CH:12]=[CH:11][C:5]2[CH2:6][S:7](=[O:10])(=[O:9])[CH2:8][C:4]=2[CH:3]=1.B1(B2OC(C)(C)C(C)(C)O2)OC(C)(C)C(C)(C)O1.CC([O-])=O.[K+].C([O-])([O-])=O.[K+].[K+].[NH2:42][C:43]1[C:48]2[CH:49]=[C:50](Br)[S:51][C:47]=2[C:46]([C:53]([NH2:55])=[O:54])=[CH:45][N:44]=1>CS(C)=O.O>[NH2:42][C:43]1[C:48]2[CH:49]=[C:50]([C:2]3[CH:12]=[CH:11][CH:5]4[CH2:6][S:7](=[O:10])(=[O:9])[CH2:8][CH:4]4[CH:3]=3)[S:51][C:47]=2[C:46]([C:53]([NH2:55])=[O:54])=[CH:45][N:44]=1

Komponenten

8

Reaktionsbedingungen

Temperatur
85 °C

Versuchsvorschrift

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).

Aufarbeitung

  1. customThe mixture was degassed with N2
  2. filtrationthen filtered
  3. washThe residue was washed with DMSO (2 mL)
  4. customthe filtrate purified by reverse phase preparative HPLC

Quellen und Nachweise

ORD-Eintrag
ord-bbc7da129029491fa8c2b79debaa811c
Quelldatensatz
uspto-grants-2009_12
Patentnummer
US07635695B2

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