Benzoyl chloride → HCID 21313390, Verbindung

HRID 2397483Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2397483
[CH:1]1([CH2:7][CH:8]2[CH2:13][CH2:12][CH2:11][CH2:10][NH:9]2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.ClCCCC(=O)CCCC.C(=O)([O-])[O-].[K+].[K+].C1(CC2CCCCN2CCCC(=O)CCCC)CCCCC1.COC1C=CC(NN)=CC=1.C1(CC2CCCCN2[CH2:75][CH2:76][C:77]2[C:85]3[C:80](=[CH:81][CH:82]=[C:83]([O:86][CH3:87])[CH:84]=3)[NH:79][C:78]=2[CH2:88][CH2:89][CH2:90][CH3:91])CCCCC1.[H-].[Na+].[Na].[C:95](Cl)(=[O:102])[C:96]1[CH:101]=[CH:100][CH:99]=[CH:98][CH:97]=1>C(O)C.CN(C=O)C>[C:95]([N:79]1[C:80]2[C:85](=[CH:84][C:83]([O:86][CH3:87])=[CH:82][CH:81]=2)[C:77]([CH2:76][CH2:75][N:9]2[CH2:10][CH2:11][CH2:12][CH2:13][CH:8]2[CH2:7][CH:1]2[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]2)=[C:78]1[CH2:88][CH2:89][CH2:90][CH3:91])(=[O:102])[C:96]1[CH:101]=[CH:100][CH:99]=[CH:98][CH:97]=1

Komponenten

12

Versuchsvorschrift

1-Benzoyl-3-[2-(2-cyclohexylmethylpiperidino)ethyl]-5-methoxy-2-butylindole is prepared by reaction of 2-cyclohexylmethylpiperidine with 1-chlorooctan-4-one in ethanol in the presence of anhydrous potassium carbonate; reaction of the resulting 1-(2-cyclohexylmethylpiperidino)octan-4-one with 4-methoxyphenylhydrazine in ethanol; and reaction of the resulting 3-[2-(2-cyclohexylmethylpiperidino)ethyl]-5-methoxy-2-butylindole with sodium hydride in DMF followed by reaction of the resulting sodium salt with benzoyl chloride all according to the procedure described above in Example 1.

Quellen und Nachweise

ORD-Eintrag
ord-bdacfe0b52424d5dafd47f68f6520661
Quelldatensatz
uspto-grants-1977_05
Patentnummer
US04021431

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