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Dichloromethane → 4-(4-But-2-ynyloxy-benzenesulfonylmethyl)-piperidine-1,4-dicarboxylic acid ethyl ester methyl ester

HRID 278340
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 278340
C([O:3][C:4]([C:6]1([CH2:12][S:13]([C:16]2[CH:21]=[CH:20][C:19]([O:22][CH2:23][C:24]#[C:25][CH3:26])=[CH:18][CH:17]=2)(=[O:15])=[O:14])[CH2:11][CH2:10][NH:9][CH2:8][CH2:7]1)=[O:5])C.[CH3:27]/[C:28](/[O:34][Si](C)(C)C)=N\[Si](C)(C)C.[CH3:39][O:40]C(Cl)=O.[CH2:44](Cl)Cl>>[CH3:44][O:3][C:4]([C:6]1([CH2:12][S:13]([C:16]2[CH:21]=[CH:20][C:19]([O:22][CH2:23][C:24]#[C:25][CH3:26])=[CH:18][CH:17]=2)(=[O:14])=[O:15])[CH2:11][CH2:10][N:9]([C:39]([O:34][CH2:28][CH3:27])=[O:40])[CH2:8][CH2:7]1)=[O:5]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 4

HCID 6344Dichloromethane3×HCID 6586Methyl chloroformateHCID 6913588N,O-bis(trimethylsilyl)acetamideHCID 22626999HCID 22626999, Verbindung

Produkt 1

HCID 538996104-(4-But-2-ynyloxy-benzenesulfonylmethyl)-piperidine-1,4-dicarboxylic acid ethyl ester methyl esterAusbeute 85 %

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

To a solution of 4-[[[4-(2-Butynyloxy)phenyl]sulfonyl]methyl]-4-piperidinecarboxylic acid ethyl ester (0.354 g, 0.85 mmol) in 1.0 mL of CH2Cl2 under N2 atmosphere was added dropwise a solution of N,O-bis(trimethylsilyl)acetamide (0.462 ml, 1.87 mmol) in 0.5 mL of CH2Cl2 and stirred for 1 h. The reaction was cooled to 0° C. and added dropwise a solution of 0.079 mL (1.02 mmol) of methylchloroformate in 0.5 mL of CH2Cl2. The reaction was allowed to stir at room temperature for 1 h and cooled to 0° C., quenched with pH 7 buffer solution and extracted with EtOAc. The organics was washed with H2O, brine, dried over MgSO4, filtered, and concentrated in vacuo. The residue was chromatographed on silica gel eluting with EtOAc:hexanes (1:2) to provide 0.315 g (85%) of the desired product as a colorless oil. Electrospray Mass Spec: 438.3 (M+H)+

Aufarbeitung

  1. stirringto stir at room temperature for 1 h
  2. temperaturecooled to 0° C.
  3. customquenched with pH 7 buffer solution
  4. extractionextracted with EtOAc
  5. washThe organics was washed with H2O, brine
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. customThe residue was chromatographed on silica gel eluting with EtOAc:hexanes (1:2)

Quellen und Nachweise

ORD-Eintrag
ord-0d9ff5fbf2c440d5a9cb5c4793af6596
Quelldatensatz
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06358980B1

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