Tetrahydrofuran → 2-(2-Amino-6-chloro-5-formyl-pyrimidin-4-ylamino)-N-(3-trifluoromethyl-phenyl)-acetamide

HRID 212866Notizen

Reaktionsgleichung

[CH2:36]1[O:37][CH2:38][CH2:39][CH2:40]1.[CH:12]([N:13]([CH2:14][CH3:15])[CH:16]([CH3:17])[CH3:18])([CH3:19])[CH3:20].[NH2:1][c:2]1[n:3][c:4]([Cl:11])[c:5]([CH:9]=[O:10])[c:6]([Cl:8])[n:7]1.[NH2:21][CH2:22][C:23](=[O:24])[NH:25][c:26]1[cH:27][c:28]([C:32]([F:33])([F:34])[F:35])[cH:29][cH:30][cH:31]1>>[NH2:1][c:2]1[n:3][c:4]([NH:21][CH2:22][C:23](=[O:24])[NH:25][c:26]2[cH:27][c:28]([C:32]([F:33])([F:34])[F:35])[cH:29][cH:30][cH:31]2)[c:5]([CH:9]=[O:10])[c:6]([Cl:8])[n:7]1

Komponenten

Edukt 4

HCID 8028Tetrahydrofuran

HCID 81531Diisopropylethylamine

HCID 2655462-Amino-4,6-dichloropyrimidine-5-carboxaldehyde

HCID 66124112-Amino-N-(3-trifluoromethyl-phenyl)-acetamide

Produkt 1

HCID 112917662-(2-Amino-6-chloro-5-formyl-pyrimidin-4-ylamino)-N-(3-trifluoromethyl-phenyl)-acetamide

Quellen und Nachweise

ORD-Eintrag: ord-73b9036be9734f108859f942a25e3ed8
Quelldatensatz: Training data from https://doi.org/10.1039/C8SC04228D (6/10)
DOI: 10.1039/C8SC04228D

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