Tetrahydrofuran → 3-[(4-Chlorophenyl)sulfonyl]-N-[2-(diethylamino)ethyl]-1-pyrrolidinecarboxamide
Reaktionsgleichung
[C:1](N1C=CN=C1)([N:3]1[CH:7]=[CH:6]N=C1)=[O:2].C(N[N:16]([CH2:20][CH3:21])NCC)C.[Cl:22][C:23]1[CH:28]=[CH:27][C:26]([S:29]([CH:32]2[CH2:36][CH2:35][NH:34][CH2:33]2)(=[O:31])=[O:30])=[CH:25][CH:24]=1.O1CC[CH2:39][CH2:38]1>>[Cl:22][C:23]1[CH:24]=[CH:25][C:26]([S:29]([CH:32]2[CH2:36][CH2:35][N:34]([C:1]([NH:3][CH2:7][CH2:6][N:16]([CH2:20][CH3:21])[CH2:38][CH3:39])=[O:2])[CH2:33]2)(=[O:30])=[O:31])=[CH:27][CH:28]=1Komponenten
5
Versuchsvorschrift
A solution of 4.93 g (0.0304 mole) of 1,1'-carbonyldiimidazole and 3.36 g (0.029 mole) of N,N-diethylaminoethylamine in 200 ml of tetrahydrofuran was stirred for 40 min at room temperature. A solution of 5.78 g (0.0236 mole) of 3-[(4-chlorophenyl)sulfonyl]pyrrolidine (free base) in tetrahydrofuran was added and the solution was refluxed overnight. The solvent was removed in vacuo and the resulting oil was dissolved in methylene chloride. The solution was extracted with several portions of water and was dried over magnesium sulfate. The solvent was removed in vacuo to give an oil residue. The residue was crystallized from a mixture of methanol, ether and hexane to give 4.28 g (46.7%) of white crystals, m.p. 86°-87.5° C.
Aufarbeitung
- temperaturethe solution was refluxed overnight
- customThe solvent was removed in vacuo
- dissolutionthe resulting oil was dissolved in methylene chloride
- extractionThe solution was extracted with several portions of water
- dry with materialwas dried over magnesium sulfate
- customThe solvent was removed in vacuo
- customto give an oil residue
- customThe residue was crystallized from a mixture of methanol, ether and hexane
Quellen und Nachweise
- ORD-Eintrag
- ord-9e0e7082c4e8441882c81387c218623e
- Quelldatensatz
- uspto-grants-1987_02
- Patentnummer
- US04642348
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