Pyridine → HCID 15521320, compound

HRID 1209908Notes

Reaction equation

HRID 1209908 reaction equation
[C:54]([OH:55])([CH3:56])([CH3:57])[CH3:58].[CH2:47]([Cl:48])[Cl:49].[CH:50]([Cl:51])([Cl:52])[Cl:53].[Cl:13][C:14]([C:15]([Cl:16])=[O:17])=[O:18].[Cl:25][c:26]1[c:27]2[c:28]([cH:29][cH:30][c:31]([I:32])[cH:33]2)[n:34][cH:35][n:36]1.[I:1][c:2]1[cH:3][c:4]2[c:5](=[O:12])[nH:6][cH:7][n:8][c:9]2[cH:10][cH:11]1.[NH2:37][c:38]1[cH:39][c:40]2[cH:41][cH:42][nH:43][c:44]2[cH:45][cH:46]1.[O:59]=[CH:60][N:61]([CH3:62])[CH3:63].[cH:19]1[cH:20][cH:21][n:22][cH:23][cH:24]1>>[I:1][c:2]1[cH:3][c:4]2[c:5]([NH:37][c:38]3[cH:39][c:40]4[cH:41][cH:42][nH:43][c:44]4[cH:45][cH:46]3)[n:6][cH:7][n:8][c:9]2[cH:10][cH:11]1

Participants

10

Reactant 9

HCID 1049PyridineHCID 6212ChloroformHCID 6228DimethylformamideHCID 6344DichloromethaneHCID 6386tert-ButanolHCID 65578Oxalyl chlorideHCID 788675-AminoindoleHCID 111738094-Chloro-6-iodoquinazolineHCID 1354016666-Iodoquinazolin-4-one

Product 1

HCID 15521320HCID 15521320, compound

Sources & evidence

ORD record
ord-ccdacc001db94b93a8a4ef5c52e34242
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (5/10)

Reaction notes

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