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Ethanol → 4-(2-Chloro-5-methoxyanilino)-7-hydroxy-5-(3-morpholinopropoxy)quinazoline

HRID 2341636
Notes
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Reaction equation

HRID 2341636 reaction equation
[CH2:1]([c:2]1[cH:3][cH:4][cH:5][cH:6][cH:7]1)[O:8][c:9]1[cH:10][c:11]([O:29][CH2:30][CH2:31][CH2:32][N:33]2[CH2:34][CH2:35][O:36][CH2:37][CH2:38]2)[c:12]2[c:13]([NH:19][c:20]3[c:21]([Cl:28])[cH:22][cH:23][c:24]([O:26][CH3:27])[cH:25]3)[n:14][cH:15][n:16][c:17]2[cH:18]1.[CH2:42]1[O:43][CH2:44][CH2:45][CH2:46]1.[CH3:39][CH2:40][OH:41].[H:47][H:48].[O:49]=[CH:50][N:51]([CH3:52])[CH3:53]>>[OH:8][c:9]1[cH:10][c:11]([O:29][CH2:30][CH2:31][CH2:32][N:33]2[CH2:34][CH2:35][O:36][CH2:37][CH2:38]2)[c:12]2[c:13]([NH:19][c:20]3[c:21]([Cl:28])[cH:22][cH:23][c:24]([O:26][CH3:27])[cH:25]3)[n:14][cH:15][n:16][c:17]2[cH:18]1
ParticipantsSources & evidenceReaction notes

Participants

6

Reactant 5

HCID 702EthanolHCID 6228DimethylformamideHCID 8028TetrahydrofuranHCID 221408327-Benzyloxy4-(2-chloro-5-methoxyanilino)-5-(3-morpholinopropoxy)quinazolineHCID 178418361HCID 178418361, compound

Product 1

HCID 135830916
4-(2-Chloro-5-methoxyanilino)-7-hydroxy-5-(3-morpholinopropoxy)quinazoline

Sources & evidence

ORD record
ord-2398dfdaf0d7408bb56cc11d2cb73d68
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (10/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes