2-Aminothiazole → HCID 85325344, compound

HRID 211078Notes

Reaction equation

HRID 211078 reaction equation
[Br:20][N:21]1[C:22](=[O:23])[CH2:24][CH2:25][C:26]1=[O:27].[CH2:53]([Cl:54])[Cl:55].[CH:28]1([CH:34]=[C:35]([C:36](=[O:37])[OH:38])[c:39]2[cH:40][c:41]([F:46])[c:42]([F:45])[cH:43][cH:44]2)[CH2:29][CH2:30][CH2:31][CH2:32][CH2:33]1.[NH2:47][c:48]1[s:49][cH:50][cH:51][n:52]1.[c:1]1([P:2]([c:3]2[cH:4][cH:5][cH:6][cH:7][cH:8]2)[c:9]2[cH:10][cH:11][cH:12][cH:13][cH:14]2)[cH:15][cH:16][cH:17][cH:18][cH:19]1>>[CH:28]1([CH:34]=[C:35]([C:36](=[O:38])[NH:47][c:48]2[s:49][cH:50][cH:51][n:52]2)[c:39]2[cH:40][c:41]([F:46])[c:42]([F:45])[cH:43][cH:44]2)[CH2:29][CH2:30][CH2:31][CH2:32][CH2:33]1

Participants

6

Reactant 5

HCID 21552-AminothiazoleHCID 6344DichloromethaneHCID 11776TriphenylphosphineHCID 67184N-bromobutanimideHCID 67482893HCID 67482893, compound

Product 1

HCID 85325344HCID 85325344, compound

Sources & evidence

ORD record
ord-1ee4fbbaffb94ef89d8ab30131edfc00
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (6/10)

Reaction notes

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