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Potassium Cation → 7-(3-Chloropropoxy)-6-methoxy-4-(2-methylindol-5-yloxy)quinazoline

HRID 212516
Notes
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Reaction equation

HRID 212516 reaction equation
[Br:25][CH2:26][CH2:27][CH2:28][Cl:29].[C:30](=[O:31])([O-:32])[O-:33].[K+:34].[K+:35].[O:37]=[CH:38][N:39]([CH3:40])[CH3:41].[OH2:36].[OH:1][c:2]1[c:3]([O:23][CH3:24])[cH:4][c:5]2[c:6]([O:12][c:13]3[cH:14][c:15]4[cH:16][c:17]([CH3:22])[nH:18][c:19]4[cH:20][cH:21]3)[n:7][cH:8][n:9][c:10]2[cH:11]1>>[O:1]([c:2]1[c:3]([O:23][CH3:24])[cH:4][c:5]2[c:6]([O:12][c:13]3[cH:14][c:15]4[cH:16][c:17]([CH3:22])[nH:18][c:19]4[cH:20][cH:21]3)[n:7][cH:8][n:9][c:10]2[cH:11]1)[CH2:26][CH2:27][CH2:28][Cl:29]
ParticipantsSources & evidenceReaction notes

Participants

7

Reactant 6

HCID 813Potassium Cation2×HCID 962WaterHCID 6228DimethylformamideHCID 80061-Bromo-3-chloropropaneHCID 19660Carbonate IonHCID 1357631087-hydroxy-6-methoxy-4-(2-methyl-1H-indol-5-yloxy)quinazoline

Product 1

HCID 22030878
7-(3-Chloropropoxy)-6-methoxy-4-(2-methylindol-5-yloxy)quinazoline

Sources & evidence

ORD record
ord-82c310aff2404ebdaee77a25563cc08e
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (6/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes