5-Bromo-2-methoxyphenol → (3S)-3-(5-Bromo-2-methoxyphenoxy)-1-methylpyrrolidine

Reaktionsgleichung

[Br:1][C:2]1[CH:3]=[CH:4][C:5]([O:9][CH3:10])=[C:6]([OH:8])[CH:7]=1.[CH3:11][N:12]1[CH2:16][CH2:15][C@H:14](O)[CH2:13]1>>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([O:9][CH3:10])=[C:6]([CH:7]=1)[O:8][C@H:14]1[CH2:15][CH2:16][N:12]([CH3:11])[CH2:13]1

Komponenten

Edukt 2

HCID 1422285-Bromo-2-methoxyphenol

HCID 6435041-Methyl-3-pyrrolidinol, (+)-

Produkt 1

HCID 66824451(3S)-3-(5-Bromo-2-methoxyphenoxy)-1-methylpyrrolidineAusbeute 30,5 %

Versuchsvorschrift

The title compound was prepared by the method outlined for Preparative Example 63 using 5-bromo-2-methoxy-phenol (1.00 g, 4.93 mmol) and (S)-1-methyl-pyrrolidin-3-ol (593 mg, 5.86 mmol) to afford titled compound as a colorless solid (430 mg, 30%). LC/MS (Method B) 1.17 min, [M+1]+ 286/288.

Aufarbeitung

customThe title compound was prepared by the method

Quellen und Nachweise

ORD-Eintrag: ord-66bc8419a9a3432087c49c0b705dc6d2
Quelldatensatz: uspto-grants-2015_01
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US08927546B2

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