Triethylamine → N-(5-(benzo[c][1,2,5]oxadiazol-5-yloxy)-2,3-dihydro-1H-inden-1-yl)propane-2-sulfonamide

HRID 473091Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 473091
CC1(C)C(C)(C)OB([C:9]2[CH:17]=[CH:16][C:12]3=[N:13][O:14][N:15]=[C:11]3[CH:10]=2)O1.[OH:19][C:20]1[CH:21]=[C:22]2[C:26](=[CH:27][CH:28]=1)[CH:25]([NH:29][S:30]([CH:33]([CH3:35])[CH3:34])(=[O:32])=[O:31])[CH2:24][CH2:23]2.C(N(CC)CC)C>C(Cl)Cl.C([O-])(=O)C.[Cu+2].C([O-])(=O)C>[N:13]1[O:14][N:15]=[C:11]2[CH:10]=[C:9]([O:19][C:20]3[CH:21]=[C:22]4[C:26](=[CH:27][CH:28]=3)[CH:25]([NH:29][S:30]([CH:33]([CH3:35])[CH3:34])(=[O:32])=[O:31])[CH2:24][CH2:23]4)[CH:17]=[CH:16][C:12]=12

Komponenten

6

Versuchsvorschrift

A mixture of 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[c][1,2,5]oxadiazole (0.313 mmol, 77 mg), N-(5-hydroxy-2,3-dihydro-1H-inden-1-yl)propane-2-sulfonamide (0.157 mmol, 40 mg), copper (II)acetate (0.157 mmol, 28.5 mg), triethylamine (0.783 mmol, 0.110 mL, 79 mg) and 4A molecular sieves (100 mg) in DCM (1 mL) was stirred at room temperature for 60 h. The reaction mixture was filtered through dicalite and the pad washed with MeOH before the filtrate was concentrated to dryness. The residue was purified by prep HPLC to give a brown film (32. mg, 5.5%). MS (ESI): m/z [M+H]+ 374.0

Aufarbeitung

  1. filtrationThe reaction mixture was filtered through dicalite
  2. washthe pad washed with MeOH before the filtrate
  3. concentrationwas concentrated to dryness
  4. customThe residue was purified by prep HPLC
  5. customto give a brown film (32. mg, 5.5%)

Quellen und Nachweise

ORD-Eintrag
ord-88de6eda68fc4e83922d2c0746be78ac
Quelldatensatz
uspto-grants-2014_01
Patentnummer
US08633237B2

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