Potassium Cation → HCID 22030643, compound

HRID 1141048Notes

Reaction equation

[C:24](=[O:25])([O-:26])[O-:27].[Cl:1][c:2]1[n:3][cH:4][n:5][c:6]2[cH:7][c:8]([O:14][CH2:15][CH2:16][CH2:17][N:18]3[CH2:19][CH2:20][CH2:21][CH2:22][CH2:23]3)[c:9]([O:12][CH3:13])[cH:10][c:11]12.[K+:28].[K+:29].[OH:30][c:31]1[cH:32][cH:33][c:34]2[nH:35][c:36]3[cH:37][cH:38][cH:39][cH:40][c:41]3[c:42]2[cH:43]1>>[c:2]1([O:30][c:31]2[cH:32][cH:33][c:34]3[nH:35][c:36]4[cH:37][cH:38][cH:39][cH:40][c:41]4[c:42]3[cH:43]2)[n:3][cH:4][n:5][c:6]2[cH:7][c:8]([O:14][CH2:15][CH2:16][CH2:17][N:18]3[CH2:19][CH2:20][CH2:21][CH2:22][CH2:23]3)[c:9]([O:12][CH3:13])[cH:10][c:11]12

Participants

Reactant 4

HCID 813Potassium Cation2×

HCID 19660Carbonate Ion

HCID 1514603-Hydroxycarbazole

HCID 110021914-Chloro-6-methoxy-7-(3-(piperidin-1-YL)propoxy)quinazoline

Product 1

HCID 22030643HCID 22030643, compound

Sources & evidence

ORD record: ord-207e944938c6479389e29147e0e107da
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (7/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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