Ethyl Acetate → HCID 178436476, compound
Reaction equation
OC1C(=O)NN=C(CCC2C=CC=CC=2)C=1.C(OC1N=NC(C(C2C=CC=CC=2)=C)=CC=1OCC1C=CC=CC=1)C1C=CC=CC=1.C([O:54][C:55]1[N:56]=[N:57][C:58]([C:69]([C:71]2[CH:76]=[CH:75][C:74]([F:77])=[CH:73][CH:72]=2)=[CH2:70])=[CH:59][C:60]=1[O:61]CC1C=CC=CC=1)C1C=CC=CC=1.C(OCC)(=O)C>O1CCCC1>[F:77][C:74]1[CH:75]=[CH:76][C:71]([CH:69]([C:58]2[CH:59]=[C:60]([OH:61])[C:55](=[O:54])[NH:56][N:57]=2)[CH3:70])=[CH:72][CH:73]=1Participants
6
Procedure
Prepared by the same method as for 4-hydroxy-6-(2-phenylethyl)pyridazin-3(2H)-one (Example 1) from 3,4-bis(benzyloxy)-6-(1-phenylethenyl)pyridazine (Intermediate 41) except that the solvent mixture used for the hydrogenation consisted of ethyl acetate and tetrahydrofuran and the product was recrystallised from a mixture of heptane and MTBE.
Workup
- customthe product was recrystallised from a mixture of heptane and MTBE
Sources & evidence
- ORD record
- ord-384b6d643a5a474aa5c6113f9ccd9594
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09290456B2
Reaction notes
Loading…