2-Aminothiazole → HCID 59252882, compound

HRID 315246Notes

Reaction equation

HRID 315246 reaction equation
[CH:36]([N:37]([CH:38]([CH3:39])[CH3:40])[CH2:41][CH3:42])([CH3:43])[CH3:44].[F:1][c:2]1[cH:3][cH:4][c:5](-[n:8]2[cH:9][cH:10][c:11]3[cH:12][c:13]([CH:17]([C:18]([C:19](=[O:20])[OH:21])([CH3:22])[CH3:23])[c:24]4[cH:25][cH:26][cH:27][cH:28][cH:29]4)[cH:14][cH:15][c:16]23)[cH:6][cH:7]1.[NH2:30][c:31]1[s:32][cH:33][cH:34][n:35]1.[O:69]=[CH:70][N:71]([CH3:72])[CH3:73].[P-:45]([F:46])([F:47])([F:48])([F:49])([F:50])[F:51].[n:52]1([O:53][C:54]([N:55]([CH3:56])[CH3:57])=[N+:58]([CH3:59])[CH3:60])[c:61]2[n:62][cH:63][cH:64][cH:65][c:66]2[n:67][n:68]1>>[F:1][c:2]1[cH:3][cH:4][c:5](-[n:8]2[cH:9][cH:10][c:11]3[cH:12][c:13]([CH:17]([C:18]([C:19](=[O:21])[NH:30][c:31]4[s:32][cH:33][cH:34][n:35]4)([CH3:22])[CH3:23])[c:24]4[cH:25][cH:26][cH:27][cH:28][cH:29]4)[cH:14][cH:15][c:16]23)[cH:6][cH:7]1

Participants

7

Reactant 6

HCID 21552-AminothiazoleHCID 6228DimethylformamideHCID 9886HexafluorophosphateHCID 81531DiisopropylethylamineHCID 4641409(Dimethylamino)-N,N-dimethyl(3H-(1,2,3)triazolo(4,5-b)pyridin-3-yloxy)methaniminiumHCID 67005978HCID 67005978, compound

Product 1

HCID 59252882HCID 59252882, compound

Sources & evidence

ORD record
ord-761acbfb0e8c4b0d8b1b7ab9926f57fe
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (8/10)

Reaction notes

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