HCID 57799490, compound → HCID 57799806, compound

HRID 2101098Notes

Reaction equation

HRID 2101098 reaction equation
Cl[C:2]1[C:11]2[C:6](=[CH:7][C:8](F)=[C:9]([O:12][CH2:13][CH2:14][O:15][CH3:16])[CH:10]=2)[CH:5]=[C:4]([NH:18][C:19]2[CH:23]=[C:22]([CH3:24])[NH:21][N:20]=2)[N:3]=1>C(O)C>[CH2:9]([O:12][C:2]1[C:11]2[C:6](=[CH:7][C:8]([O:15][CH2:14][CH3:13])=[C:9]([O:12][CH2:13][CH2:14][O:15][CH3:16])[CH:10]=2)[CH:5]=[C:4]([NH:18][C:19]2[CH:23]=[C:22]([CH3:24])[NH:21][N:20]=2)[N:3]=1)[CH3:8]

Participants

3

Reactant 1

HCID 57799490HCID 57799490, compound

Product 1

HCID 57799806HCID 57799806, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

Similar procedure as described in example 10 was used, starting from [1-Chloro-6-fluoro-7-(2-methoxy-ethoxy)-isoquinolin-3-yl]-(5-methyl-1H-pyrazol-3-yl)-amine and ethanol to give [1,6-Diethoxy-7-(2-methoxy-ethoxy)-isoquinolin-3-yl]-(5-methyl-1H-pyrazol-3-yl)-amine. LC-MS m/e 387(MH+).

Sources & evidence

ORD record
ord-2b252b35c8794ef8bb546bf0ffdd2e6c
Source dataset
uspto-grants-2009_08
Patent number
US07572809B2

Reaction notes

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