HCID 11531559, compound → HCID 11715743, compound
Reaction equation
ClC1C=CC=C(Cl)C=1C[O:5][C:6]1[CH:15]=[C:14]2[C:9]([C:10](=[O:22])[CH:11]=[C:12]([N:16]3[CH2:21][CH2:20][O:19][CH2:18][CH2:17]3)[O:13]2)=[CH:8][CH:7]=1>CO.[Pd]>[OH:5][C:6]1[CH:15]=[C:14]2[C:9]([C:10](=[O:22])[CH:11]=[C:12]([N:16]3[CH2:17][CH2:18][O:19][CH2:20][CH2:21]3)[O:13]2)=[CH:8][CH:7]=1Participants
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
To a mixture of 7-(2,6-dichlorobenzyloxy)-2-(morpholin-4-yl)-chromen-4-one (6.60 g, 16.2 mmol) (299) and 10% Pd/C (150 mg) was added methanol (150 ml), under nitrogen. The suspension was stirred under an atmosphere of hydrogen for 40 h. The catalyst was removed by filtration through Celite, washing with methanol. The solvent was removed by evaporation in vacuo to provide an off-white solid. This was treated with fresh catalyst, re-suspended in methanol under nitrogen and stirred under an atmosphere of hydrogen for a further 72 h. The catalyst was removed by filtration through Celite, washing with methanol. The filtrate was evaporated in vacuo and the crude product re-crystallised from methanol to provide 2.26 g (9.1 mmol, 57%) of the desired compound as a white solid. mp>250° C. (decomp). 1H NMR (200 Mhz, d6-DMSO) δ 3.78 (4H, m); 3.86 (4H, m); 6.15 (1H, s); 7.05-7.13 (2H, m); 7.93 (1H, d); 11.3 (1H, bs). ESMS m/z=247 (M+), 190, 105.
Workup
- customThe catalyst was removed by filtration through Celite
- washwashing with methanol
- customThe solvent was removed by evaporation in vacuo
- customto provide an off-white solid
- additionThis was treated with fresh catalyst
- stirringstirred under an atmosphere of hydrogen for a further 72 h
- customThe catalyst was removed by filtration through Celite
- washwashing with methanol
- customThe filtrate was evaporated in vacuo
- customthe crude product re-crystallised from methanol
Sources & evidence
- ORD record
- ord-83f453932f0a460a8586bbafddc84412
- Source dataset
- uspto-grants-2007_06
- Patent number
- US07226918B2
Reaction notes
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