Potassium Cation → 5-(2-Phthalimidoethylamino)-1,3,6-trimethylpyrimidine-2,4(1H,3H)-dione

Reaction equation

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

Participants

Reactant 5

HCID 813Potassium Cation2×

HCID 6342Acetonitrile

HCID 113251H-Isoindole-1,3(2H)-dione, 2-(2-bromoethyl)-

HCID 19660Carbonate Ion

HCID 816935AB-323/25048145

Product 1

HCID 128188675-(2-Phthalimidoethylamino)-1,3,6-trimethylpyrimidine-2,4(1H,3H)-dione

Sources & evidence

ORD record: ord-ad85767878b0406eb3fe28c7c707a560
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (3/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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