![[(1S,3S)-3-[[4-Methoxy-3-(3-methoxypropoxy)phenyl]methyl]-4-methyl-1-[(2S, 4S)-tetrahydro-4-(1-met…](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FFM25237.webp&w=3840&q=75)
[(1S,3S)-3-[[4-Methoxy-3-(3-methoxypropoxy)phenyl]methyl]-4-methyl-1-[(2S, 4S)-tetrahydro-4-(1-methylethyl)-5-oxo-2-furanyl]pentyl]c arbamic acid 1,1-tert-butyl ester
CAS:
Ref. 3D-FM25237
Produktinformation
Name:[(1S,3S)-3-[[4-Methoxy-3-(3-methoxypropoxy)phenyl]methyl]-4-methyl-1-[(2S, 4S)-tetrahydro-4-(1-methylethyl)-5-oxo-2-furanyl]pentyl]c arbamic acid 1,1-tert-butyl ester
Synonyme:
- N-[(1S,3S)-3-[[4-Methoxy-3-(3-methoxypropoxy)phenyl]methyl]-4-methyl-1-[(2S
- 4S)-tetrahydro-4-(1-methylethyl)-5-oxo-2-furanyl]pentyl ]carbamic acid 1,1-dimethylethyl ester
Marke:Biosynth
Beschreibung:[(1S,3S)-3-[[4-Methoxy-3-(3-methoxypropoxy)phenyl]methyl]-4-methyl-1-[(2S, 4S)-tetrahydro-4-(1-methylethyl)-5-oxo-2-furanyl]pentyl]car bamic acid 1,1-tert-butyl ester is a chiral building block that has been used in the scalable synthesis of various pharmaceuticals. The synthesis begins with ammonolysis of an amino chloride and chloroacetate. This reaction is followed by acetate extraction to yield the desired product. This process can be optimized by ring opening, magnesium removal and alkylation of aromatic hydrocarbons. The final reaction is the Suzuki coupling reaction with chromatographic purification.
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Chemische Eigenschaften
Molekulargewicht:535.71 g/mol
Formel:C30H49NO7
Reinheit:Min. 95%