Hydrochloric Acid → 6-Cyano-4-(1H-indol-5-yloxy)-7-(piperidin-4-yl)methyloxyquinoline

HRID 2348173Notes

Reaction equation

HRID 2348173 reaction equation
[C:1](#[N:2])[c:3]1[cH:4][c:5]2[c:6]([O:29][c:30]3[cH:31][c:32]4[cH:33][cH:34][nH:35][c:36]4[cH:37][cH:38]3)[cH:7][cH:8][n:9][c:10]2[cH:11][c:12]1[O:13][CH2:14][CH:15]1[CH2:16][CH2:17][N:18]([O:21][C:22]([O:23][C:24]([CH3:25])([CH3:26])[CH3:27])=[O:28])[CH2:19][CH2:20]1.[CH3:40][CH2:41][OH:42].[ClH:39].[O:43]1[CH2:44][CH2:45][CH2:46][CH2:47]1>>[C:1](#[N:2])[c:3]1[cH:4][c:5]2[c:6]([O:29][c:30]3[cH:31][c:32]4[cH:33][cH:34][nH:35][c:36]4[cH:37][cH:38]3)[cH:7][cH:8][n:9][c:10]2[cH:11][c:12]1[O:13][CH2:14][CH:15]1[CH2:16][CH2:17][NH:18][CH2:19][CH2:20]1

Participants

5

Reactant 4

HCID 313Hydrochloric AcidHCID 702EthanolHCID 8028TetrahydrofuranHCID 672017656-Cyano-4-(1H-indol-5-yloxy)-7-[(1-(t-butoxycarbonyloxy)piperidin-4-yl)methyloxy]quinoline

Product 1

HCID 229366766-Cyano-4-(1H-indol-5-yloxy)-7-(piperidin-4-yl)methyloxyquinoline

Sources & evidence

ORD record
ord-b3f62174214c4005a81a60b4042163a0
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (10/10)

Reaction notes

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