Potassium Cation → 2-(6-Amino-5,6,7,8-tetrahydronaphthalen-2-ylsulfanyl)-2-methylpropionic acid tert-butyl ester

HRID 109573

Reaktionsgleichung

[BH4-:31].[Br:20][C:21]([C:22](=[O:23])[O:24][C:25]([CH3:26])([CH3:27])[CH3:28])([CH3:29])[CH3:30].[CH3:33][OH:34].[K+:19].[NH2:1][CH:2]1[CH2:3][c:4]2[cH:5][cH:6][c:7]([S:12][C:13](=[O:14])[N:15]([CH3:16])[CH3:17])[cH:8][c:9]2[CH2:10][CH2:11]1.[Na+:32].[OH-:18]>>[NH2:1][CH:2]1[CH2:3][c:4]2[cH:5][cH:6][c:7]([S:12][C:21]([C:22](=[O:23])[O:24][C:25]([CH3:26])([CH3:27])[CH3:28])([CH3:29])[CH3:30])[cH:8][c:9]2[CH2:10][CH2:11]1

Komponenten

Edukt 7

HCID 813Potassium Cation

HCID 887Methanol

HCID 923Sodium ion

HCID 961Hydroxide

HCID 28123Borohydride

HCID 90290tert-Butyl 2-bromo-2-methylpropionate

HCID 86594048dimethylthiocarbamic acid S-[6-amino-5,6,7,8-tetrahydronaphthalen-2-yl) ester

Produkt 1

HCID 688599032-(6-Amino-5,6,7,8-tetrahydronaphthalen-2-ylsulfanyl)-2-methylpropionic acid tert-butyl ester

Quellen und Nachweise

ORD-Eintrag: ord-97fb8a254566438db9a27f9d29a06735
Quelldatensatz: Training data from https://doi.org/10.1039/C8SC04228D (2/10)
DOI: 10.1039/C8SC04228D

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