p-Aminoacetophenone → Hydrochloric Acid

Reaction equation

[Cl:1][c:2]1[n:3][c:4](-[c:15]2[cH:16][cH:17][cH:18][cH:19][cH:20]2)[cH:5][c:6]([N:8]2[CH2:9][CH2:10][CH:11]([OH:14])[CH2:12][CH2:13]2)[n:7]1.[NH2:21][c:22]1[cH:23][cH:24][c:25]([C:28]([CH3:29])=[O:30])[cH:26][cH:27]1>>[ClH:1].[c:2]1([NH:21][c:22]2[cH:23][cH:24][c:25]([C:28]([CH3:29])=[O:30])[cH:26][cH:27]2)[n:3][c:4](-[c:15]2[cH:16][cH:17][cH:18][cH:19][cH:20]2)[cH:5][c:6]([N:8]2[CH2:9][CH2:10][CH:11]([OH:14])[CH2:12][CH2:13]2)[n:7]1

Participants

Reactant 2

HCID 7468p-Aminoacetophenone

HCID 586260781-(2-Chloro-6-phenyl-pyrimidin-4-yl)-piperidin-4-ol

Product 2

HCID 313Hydrochloric Acid

HCID 115174791-[4-[[4-(4-Hydroxypiperidin-1-yl)-6-phenylpyrimidin-2-yl]amino]phenyl]ethanone

Sources & evidence

ORD record: ord-76bc4bbebd1541db9b718045d45eb08a
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (3/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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