HCID 25232704, compound → HCID 25232895, compound

HRID 2265010Notes

Reaction equation

HRID 2265010 reaction equation
CN(C[C:5]1[N:6]2[CH:12]=[C:11]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=3[NH2:19])[N:10]=[C:7]2[S:8][CH:9]=1)C.[N+](C1C=CC=CC=1C1N=[C:31]2[N:35]([CH:36]=1)[CH:34]=C(CO)S2)([O-])=O>>[CH3:34][N:35]([CH2:36][C:9]1[S:8][C:7]2=[N:10][C:11]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=3[NH2:19])=[CH:12][N:6]2[CH:5]=1)[CH3:31]

Participants

3

Reactant 2

HCID 25232704HCID 25232704, compoundHCID 25232894HCID 25232894, compound

Product 1

HCID 25232895HCID 25232895, compound

Procedure

Essentially the same procedure used during the preparation of 2-(3-dimethylaminomethyl-imidazo[2,1-b]thiazol-6-yl)-phenylamine was employed, except that [6-(2-nitro-phenyl)-imidazo[2,1-b]thiazol-2-yl]-methanol was used as the starting material.

Sources & evidence

ORD record
ord-2afd44261742445496cdca9f9f9c52a3
Source dataset
uspto-grants-2010_12
Patent number
US07855289B2

Reaction notes

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