Hydrogen Bromide → Tert-butyl 3-(6-hydroxy-3,4-dihydroisoquinolin-2(1H)-yl)propanoate

Reaktionsgleichung

[BrH:1].[C:13]([CH:14]=[CH2:15])(=[O:16])[O:17][C:18]([CH3:19])([CH3:20])[CH3:21].[CH2:22]([N:23]([CH:24]([CH3:25])[CH3:26])[CH:27]([CH3:28])[CH3:29])[CH3:30].[CH2:2]1[NH:3][CH2:4][CH2:5][c:6]2[cH:7][c:8]([OH:12])[cH:9][cH:10][c:11]21.[CH3:31][OH:32]>>[CH2:2]1[N:3]([CH2:15][CH2:14][C:13](=[O:16])[O:17][C:18]([CH3:19])([CH3:20])[CH3:21])[CH2:4][CH2:5][c:6]2[cH:7][c:8]([OH:12])[cH:9][cH:10][c:11]21

Komponenten

Edukt 5

HCID 260Hydrogen Bromide

HCID 887Methanol

HCID 15458tert-Butyl acrylate

HCID 266981,2,3,4-Tetrahydroisoquinolin-6-ol

HCID 81531Diisopropylethylamine

Produkt 1

HCID 59595894Tert-butyl 3-(6-hydroxy-3,4-dihydroisoquinolin-2(1H)-yl)propanoate

Quellen und Nachweise

ORD-Eintrag: ord-d34c03e6a7fd4c9f8ee1ae3788820b86
Quelldatensatz: Training data from https://doi.org/10.1039/C8SC04228D (2/10)
DOI: 10.1039/C8SC04228D

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