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Potassium Cation → 4-(Chloro-2-fluoroanilino)-6-methoxy-7-(3-tetrahydropyran-2-yloxypropoxy)quinazoline

HRID 296558
Notes
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Reaction equation

HRID 296558 reaction equation
[Br:23][CH2:24][CH2:25][CH2:26][O:27][CH:28]1[O:29][CH2:30][CH2:31][CH2:32][CH2:33]1.[C:34](=[O:35])([O-:36])[O-:37].[Cl:1][N:2]([c:3]1[c:4]([F:9])[cH:5][cH:6][cH:7][cH:8]1)[c:10]1[n:11][cH:12][n:13][c:14]2[cH:15][c:16]([OH:22])[c:17]([O:20][CH3:21])[cH:18][c:19]12.[K+:38].[K+:39].[O:40]=[CH:41][N:42]([CH3:43])[CH3:44].[OH2:45]>>[Cl:1][N:2]([c:3]1[c:4]([F:9])[cH:5][cH:6][cH:7][cH:8]1)[c:10]1[n:11][cH:12][n:13][c:14]2[cH:15][c:16]([O:22][CH2:24][CH2:25][CH2:26][O:27][CH:28]3[O:29][CH2:30][CH2:31][CH2:32][CH2:33]3)[c:17]([O:20][CH3:21])[cH:18][c:19]12
ParticipantsSources & evidenceReaction notes

Participants

7

Reactant 6

HCID 813Potassium Cation2×HCID 962WaterHCID 6228DimethylformamideHCID 19660Carbonate IonHCID 27779882-(3-Bromopropoxy)tetrahydro-2H-pyranHCID 1359906824-(Chloro-2-fluoroanilino)7-hydroxy-6-methoxyquinazoline

Product 1

HCID 18753424
4-(Chloro-2-fluoroanilino)-6-methoxy-7-(3-tetrahydropyran-2-yloxypropoxy)quinazoline

Sources & evidence

ORD record
ord-18b71031b13141f29d7bf3ebbe1a72bc
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (8/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes