Ethyl 7-bromoheptanoate → 8-Carbamoyl-12-hydroxy-3-methylheptadecanoic acid
Reaktionsgleichung
BrCCCCCCC(OCC)=O.[CH3:13][CH:14]([CH2:20][CH2:21][CH2:22][CH2:23]I)[CH2:15][C:16]([O:18]C)=[O:17].COC(CC(C)CCCCC(C(OC(C)(C)C)=O)C(OC(C)(C)C)=O)=O.C(OC(CCCCC)CCCC(CCCCC(C)CC(OC)=O)(C([O-])=O)C(OC(C)(C)C)=O)(=O)C.C(C(CCCC(OC(=O)C)CCCCC)CCCCC(C)CC(OC)=O)(O)=O.[C:114]([CH:117]([CH2:129][CH2:130][CH2:131][C@@H:132]([O:138]C(=O)C)[CH2:133][CH2:134][CH2:135][CH2:136][CH3:137])CCCCCCC(OCC)=O)(=[O:116])[NH2:115].C(C(CCCCCC(C(=O)N)CCC[C@@H](O)CCCCC)C(O)=O)C>>[C:114]([CH:117]([CH2:129][CH2:130][CH2:131][CH:132]([OH:138])[CH2:133][CH2:134][CH2:135][CH2:136][CH3:137])[CH2:23][CH2:22][CH2:21][CH2:20][CH:14]([CH3:13])[CH2:15][C:16]([OH:18])=[O:17])(=[O:116])[NH2:115]Komponenten
8
Edukt 7
Produkt 1
Versuchsvorschrift
The synthesis of this compound is carried out as described in Example 1 except that, in Step A, the ethyl 7-bromoheptanoate is replaced by an equimolar amount of methyl 3-methyl-7-iodoheptanoate. The product of Step A is thus: di-tert.-butyl (6-methoxycarbonyl-5-methylhexyl)malonate. Subsequent steps yield: di.-tert.-butyl 2-(4-acetoxynonyl)-2-(6-methoxycarbonyl-5-methylhexyl)malonate (D); methyl 8carboxy-12-acetoxy-3-methylheptadecanoate (V); methyl 8-chlorocarbonyl-12-acetoxy-3-methylheptadecanoate (D); methyl 8-carbamoyl-12-acetoxy-3-methylheptadecanote (E); and 8carbamoyl-12-acetoxy-3-methylheptadecanoic acid (F).
Aufarbeitung
- customThe synthesis of this compound
Quellen und Nachweise
- ORD-Eintrag
- ord-f5ad0926191d484091dc4ea1e159b25c
- Quelldatensatz
- uspto-grants-1977_10
- Patentnummer
- US04055597
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