4-Quinolinecarboxaldehyde → HCID 178430394, compound

HRID 675035Notes

Reaction equation

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

Participants

Reactant 2

HCID 780724-Quinolinecarboxaldehyde

HCID 1363442076-[4-methyl-1-[(2-methylpyrimidin-5-yl)methyl]pyrrolidin-3-yl]-1-(oxan-4-yl)-5H-pyrazolo[5,4-d]pyrimidin-4-one

Product 1

HCID 178430394HCID 178430394, compound

Sources & evidence

ORD record: ord-5e6948f5bb454d3da8cedbba4536f899
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (3/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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