1,2-Dichloroethane → 5-[(2-oxo-2,3-dihydro-1H-indol-4-ylmethyl)-carbamoyl]-3-trifluoromethyl-thiophene-2-carboxylic acid methyl ester

HRID 1952601Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1952601
[CH3:1][O:2][C:3]([C:5]1[S:6][C:7]([C:14]([OH:16])=O)=[CH:8][C:9]=1[C:10]([F:13])([F:12])[F:11])=[O:4].C(N(CC)CC)C.C(Cl)CCl.C1C=CC2N(O)N=NC=2C=1.Cl.[NH2:39][CH2:40][C:41]1[CH:49]=[CH:48][CH:47]=[C:46]2[C:42]=1[CH2:43][C:44](=[O:50])[NH:45]2>CN(C=O)C>[CH3:1][O:2][C:3]([C:5]1[S:6][C:7]([C:14](=[O:16])[NH:39][CH2:40][C:41]2[CH:49]=[CH:48][CH:47]=[C:46]3[C:42]=2[CH2:43][C:44](=[O:50])[NH:45]3)=[CH:8][C:9]=1[C:10]([F:11])([F:12])[F:13])=[O:4]

Komponenten

7

Versuchsvorschrift

To a solution of 3-Trifluoromethyl-thiophene-2,5-dicarboxylic acid 2-methyl ester (590 mg, 2.32 mmol) in anhydrous DMF (10 mL) was added triethylamine (1.62 mL, 11.6 mmol), EDC (530 mg, 2.78 mmol), HOBT (380 mg, 2.78 mmol), and 4-Aminomethyl-1,3-dihydro-indol-2-one hydrochloride (550 mg, 2.78 mmol). The mixture was stirred at room temperature 15 h, then quenched by pouring into EtOAc. The organic layer was washed with brine, dried over Na2SO4 and concentrated under reduced pressure. The residue was purified by flash chromatography with 0-90% EtOAc in hexane to afford the desired product (0.27 g, 29% yield).

Aufarbeitung

  1. customquenched
  2. additionby pouring into EtOAc
  3. washThe organic layer was washed with brine
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was purified by flash chromatography with 0-90% EtOAc in hexane

Quellen und Nachweise

ORD-Eintrag
ord-044c5f7a258545b0aa938e8af1105b55
Quelldatensatz
uspto-grants-2013_03
Patentnummer
US08404859B2

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