Sodium Iodide → 5-(4-Methylsulfonyl-phenyl)-1''-[(1-trifluoromethyl-cyclopropyl)-methyl]-dispiro[2,3-dihydrofuro[2,3-c]pyridine-2,1'-cyclobutane-3',4''-piperidine]

HRID 2406341Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2406341
[F:1][C:2]([F:13])([F:12])[C:3]1([CH2:6]OS(C)(=O)=O)[CH2:5][CH2:4]1.[I-].[Na+].[CH3:16][S:17]([C:20]1[CH:25]=[CH:24][C:23]([C:26]2[CH:27]=[C:28]3[CH2:42][C:33]4([CH2:41][C:35]5([CH2:40][CH2:39][NH:38][CH2:37][CH2:36]5)[CH2:34]4)[O:32][C:29]3=[CH:30][N:31]=2)=[CH:22][CH:21]=1)(=[O:19])=[O:18].C([O-])([O-])=O.[K+].[K+]>CN(C)C=O.O>[CH3:16][S:17]([C:20]1[CH:25]=[CH:24][C:23]([C:26]2[CH:27]=[C:28]3[CH2:42][C:33]4([CH2:41][C:35]5([CH2:36][CH2:37][N:38]([CH2:6][C:3]6([C:2]([F:1])([F:12])[F:13])[CH2:4][CH2:5]6)[CH2:39][CH2:40]5)[CH2:34]4)[O:32][C:29]3=[CH:30][N:31]=2)=[CH:22][CH:21]=1)(=[O:19])=[O:18]

Komponenten

7

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

A solution of methanesulfonic acid (1-trifluoromethyl-cyclopropyl)methyl ester (45 mg) and sodium iodide (34 mg) in N,N-dimethylformamide (2 mL) is stirred at room temperature for 4 h. 5-(4-Methylsulfonyl-phenyl)-dispiro[2,3-dihydrofuro[2,3-c]pyridine-2,1′-cyclobutane-3′,4″-piperidine] (HCl salt; 50 mg) and K2CO3 (35 mg) are added and the resulting mixture is heated to 60° C. After stirring the mixture at 60° C. for 4 h, water is added and the mixture is extracted with ethyl acetate. The combined extracts are dried (Na2SO4) and concentrated. The residue is triturated with methanol to give the title compound. LC (method 1): tR=0.82 min; Mass spectrum (ESI+): m/z=507 [M+H]+.

Aufarbeitung

  1. extractionthe mixture is extracted with ethyl acetate
  2. dry with materialThe combined extracts are dried (Na2SO4)
  3. concentrationconcentrated
  4. customThe residue is triturated with methanol

Quellen und Nachweise

ORD-Eintrag
ord-bc3af0339b074e86b8ffb4d69282f849
Quelldatensatz
uspto-grants-2014_08
Patentnummer
US08809361B2

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