![[(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
Informations sur le produit
Nom:[(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
Synonymes :
- 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
Marque:Biosynth
Description :[(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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Propriétés chimiques
Masse moléculaire :535.71 g/mol
Formule :C30H49NO7
Degré de pureté :Min. 95%