Reaktionsgleichung
[Li+].C[Si]([N-:6][Si](C)(C)C)(C)C.N1(CCO[C:20]2[CH:34]=[CH:33][C:23]3[N:24]=[C:25]([CH2:27][C:28]([O:30]CC)=O)[NH:26][C:22]=3[CH:21]=2)CCOCC1.[NH2:35][C:36]1[CH:41]=[CH:40][C:39]([Cl:42])=[CH:38][C:37]=1[C:43]#[N:44].[CH2:45]1[CH2:49][O:48][CH2:47][CH2:46]1>>[Cl:42][C:39]1[CH:40]=[CH:41][C:36]([NH:35][C:28](=[O:30])[CH2:27][C:25]2[NH:26][C:22]3[CH:21]=[C:20]([N:6]4[CH2:45][CH2:49][O:48][CH2:47][CH2:46]4)[CH:34]=[CH:33][C:23]=3[N:24]=2)=[C:37]([C:43]#[N:44])[CH:38]=1Komponenten
5
Reaktionsbedingungen
- Temperatur
- 23 °C
Versuchsvorschrift
LiHMDS (2.5 eq) was added to ethyl 2-[5-(2-morpholin-4-ylethoxy)benzimidazol-2-yl]acetate (1.0 eq) in THF at −78° C. After 1 hour, 2-amino-5-chlorobenzenecarbonitrile (0.82 eq) in THF was added. The reaction was allowed to warm to 23° C. and stirred overnight. The resulting mixture was quenched with NH4Cl (aqueous saturated solution) and extracted with EtOAc. The combined organic layers were washed with H2O and brine, dried over Na2SO4, filtered and concentrated in vacuo to yield a brown solid. The crude material was purified by silica gel chromatography (5:1 EtOAc:hexane) to give the desired product. LC/MS m/z 396.1 (MH+), Rt 1.79 minutes.
Aufarbeitung
- customThe resulting mixture was quenched with NH4Cl (aqueous saturated solution)
- extractionextracted with EtOAc
- washThe combined organic layers were washed with H2O and brine
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated in vacuo
- customto yield a brown solid
- customThe crude material was purified by silica gel chromatography (5:1 EtOAc:hexane)
Quellen und Nachweise
- ORD-Eintrag
- ord-ee75b53d91664d5d938cc736289afa5f
- Quelldatensatz
- uspto-grants-2004_07
- Patentnummer
- US06762194B2
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