6-(1-Ethoxyvinyl)-3-((6-fluoro-1-methyl-1H-indazol-5-yl)methyl)imidazo[1,2-b]pyridazine → HCID 58190513, compound

HRID 456152Notes

Reaction equation

HRID 456152 reaction equation
[F:1][C:2]1[CH:10]=[C:9]2[C:5]([CH:6]=[N:7][N:8]2[CH3:11])=[CH:4][C:3]=1[CH:12]([C:14]1[N:18]2[N:19]=[C:20]([C:23](=[O:25])[CH3:24])[CH:21]=[CH:22][C:17]2=[N:16][CH:15]=1)C.C(OC(C1C=CC2N(C(CC3C=C4C(=CC=3F)N(C)N=C4)=CN=2)N=1)=C)C>>[F:1][C:2]1[CH:10]=[C:9]2[C:5]([CH:6]=[N:7][N:8]2[CH3:11])=[CH:4][C:3]=1[CH2:12][C:14]1[N:18]2[N:19]=[C:20]([C:23](=[O:25])[CH3:24])[CH:21]=[CH:22][C:17]2=[N:16][CH:15]=1

Participants

3

Reactant 2

HCID 581905506-(1-Ethoxyvinyl)-3-((6-fluoro-1-methyl-1H-indazol-5-yl)methyl)imidazo[1,2-b]pyridazineHCID 581905981-(3-(1-(6-Fluoro-1-methyl-1H-indazol-5-yl)ethyl)imidazo[1,2-b]pyridazin-6-yl)ethanone

Product 1

HCID 58190513HCID 58190513, compound

Procedure

The title compound was prepared as a white solid in analogy to the synthesis of compound 68.4 from 6-(1-ethoxyvinyl)-3-((6-fluoro-1-methyl-1H-indazol-5-yl)methyl)imidazo[1,2-b]pyridazine. LCMS (method B): [MH]+=324, tR=2.41 min.

Sources & evidence

ORD record
ord-560e09be9bf2467287402c9c5573a846
Source dataset
uspto-grants-2013_07
Patent number
US08497368B2

Reaction notes

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