Potassium Cation → Tert-butyl 1-(4-methoxycarbonylphenyl)-5-propylsulfanyl-pyrazole-4-carboxylate

HRID 111942Notizen

Reaktionsgleichung

[C:24](=[O:25])([O-:26])[O-:27].[CH2:30]([CH2:31][CH3:32])[SH:33].[CH3:34][CH2:35][O:36][C:37](=[O:38])[CH3:39].[CH3:40][CH2:41][CH2:42][C:43]#[N:44].[Cl:1][c:2]1[c:3]([C:17](=[O:18])[O:19][C:20]([CH3:21])([CH3:22])[CH3:23])[cH:4][n:5][n:6]1-[c:7]1[cH:8][cH:9][c:10]([C:13](=[O:14])[O:15][CH3:16])[cH:11][cH:12]1.[K+:28].[K+:29]>>[c:2]1([S:33][CH2:30][CH2:31][CH3:32])[c:3]([C:17](=[O:18])[O:19][C:20]([CH3:21])([CH3:22])[CH3:23])[cH:4][n:5][n:6]1-[c:7]1[cH:8][cH:9][c:10]([C:13](=[O:14])[O:15][CH3:16])[cH:11][cH:12]1

Komponenten

Edukt 6

HCID 813Potassium Cation2×

HCID 7848Propyl mercaptan

HCID 8008Butyronitrile

HCID 8857Ethyl Acetate

HCID 19660Carbonate Ion

HCID 57437894Tert-butyl 5-chloro-1-(4-methoxycarbonylphenyl)pyrazole-4-carboxylate

Produkt 1

HCID 59516064Tert-butyl 1-(4-methoxycarbonylphenyl)-5-propylsulfanyl-pyrazole-4-carboxylate

Quellen und Nachweise

ORD-Eintrag: ord-1eb825c739f24fd588f76e47d24642fc
Quelldatensatz: Training data from https://doi.org/10.1039/C8SC04228D (2/10)
DOI: 10.1039/C8SC04228D

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