Tetrahydrofuran → N-tert-Butyl-2-methylsulfanyl-2-(3-trimethylsilanylethynyl-quinolin-6-yloxy)-acetamide

HRID 191878Notizen

Reaktionsgleichung

[Br:1][c:2]1[cH:3][n:4][c:5]2[cH:6][cH:7][c:8]([O:12][CH:13]([C:14](=[O:15])[NH:16][C:17]([CH3:18])([CH3:19])[CH3:20])[S:21][CH3:22])[cH:9][c:10]2[cH:11]1.[CH2:29]1[O:30][CH2:31][CH2:32][CH2:33]1.[CH3:23][Si:24]([CH3:25])([CH3:26])[C:27]#[CH:28].[CH3:34][CH2:35][O:36][C:37](=[O:38])[CH3:39].[Cu:41].[I:40]>>[c:2]1([C:28]#[C:27][Si:24]([CH3:23])([CH3:25])[CH3:26])[cH:3][n:4][c:5]2[cH:6][cH:7][c:8]([O:12][CH:13]([C:14](=[O:15])[NH:16][C:17]([CH3:18])([CH3:19])[CH3:20])[S:21][CH3:22])[cH:9][c:10]2[cH:11]1

Komponenten

Edukt 6

HCID 8028Tetrahydrofuran

HCID 8857Ethyl Acetate

HCID 23978Copper

HCID 24841Hydrogen iodide

HCID 66111Trimethylsilylacetylene

HCID 667517422-(3-bromoquinolin-6-yl)oxy-N-tert-butyl-2-methylsulfanylacetamide

Produkt 1

HCID 59565338N-tert-Butyl-2-methylsulfanyl-2-(3-trimethylsilanylethynyl-quinolin-6-yloxy)-acetamide

Quellen und Nachweise

ORD-Eintrag: ord-00a51ac01163479fbd9c97063d3ccc79
Quelldatensatz: Training data from https://doi.org/10.1039/C8SC04228D (6/10)
DOI: 10.1039/C8SC04228D

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