3,4-bis(Benzyloxy)-6-[(3-fluorophenyl)methyl]pyridazine → HCID 178518798, compound

HRID 927164Notes

Reaction equation

HRID 927164 reaction equation
OC1C(=O)NN=C(CCC2C=CC=CC=2)C=1.C([O:24][C:25]1[N:26]=[N:27][C:28]([CH2:39][C:40]2[CH:45]=[CH:44][CH:43]=[C:42]([F:46])[CH:41]=2)=[CH:29][C:30]=1[O:31]CC1C=CC=CC=1)C1C=CC=CC=1>C(O)C>[F:46][C:42]1[CH:41]=[C:40]([CH:45]=[CH:44][CH:43]=1)[CH2:39][C:28]1[CH:29]=[C:30]([OH:31])[C:25](=[O:24])[NH:26][N:27]=1

Participants

4

Reactant 2

HCID 712704603,4-bis(Benzyloxy)-6-[(3-fluorophenyl)methyl]pyridazine2×HCID 1785188083-Hydroxy-6-(2-Phenylethyl)pyridazin-4(1h)-One

Product 1

HCID 178518798HCID 178518798, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

Prepared in the same way as 4-hydroxy-6-(2-phenylethyl)pyridazin-3(2H)-one (Example 1) from 3,4-bis(benzyloxy)-6-[(3-fluorophenyl)methyl]pyridazine (Intermediate 54) except that the solvent used for the hydrogenation was ethanol and the product was recrystallised from a mixture of MTBE and heptanes.

Workup

  1. customthe product was recrystallised from a mixture of MTBE and heptanes

Sources & evidence

ORD record
ord-2883d712c3434ba48b81d0228b320a74
Source dataset
uspto-grants-2016_03
Patent number
US09290456B2

Reaction notes

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