benzyl 5-[(N-benzyloxycarbonyl-L-alanyl)aminomethyl]-3,6-dimethoxy-9,9-dimethylxanthene-4-acetate → 5-(L-alanylaminomethyl)-3,6-dimethoxy-9,9-dimethylxanthene-4-acetic acid
Reaction equation
C(OC([NH:11][C@H:12]([C:14]([NH:16][CH2:17][C:18]1[C:31]([O:32][CH3:33])=[CH:30][CH:29]=[C:28]2[C:19]=1[O:20][C:21]1[C:22]([CH2:38][C:39]([O:41]CC3C=CC=CC=3)=[O:40])=[C:23]([O:36][CH3:37])[CH:24]=[CH:25][C:26]=1[C:27]2([CH3:35])[CH3:34])=[O:15])[CH3:13])=O)C1C=CC=CC=1>C(O)C(F)(F)F.[Pd]>[NH2:11][C@H:12]([C:14]([NH:16][CH2:17][C:18]1[C:31]([O:32][CH3:33])=[CH:30][CH:29]=[C:28]2[C:19]=1[O:20][C:21]1[C:22]([CH2:38][C:39]([OH:41])=[O:40])=[C:23]([O:36][CH3:37])[CH:24]=[CH:25][C:26]=1[C:27]2([CH3:35])[CH3:34])=[O:15])[CH3:13]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of 0.3 g of benzyl 5-[(N-benzyloxycarbonyl-L -alanyl)aminomethyl]-3,6-dimethoxy-9,9-dimethylxanthene-4-acetate in 85 ml of trifluoroethanol was stirred under hydrogen for 15 minutes in the presence of palladium/charcoal (10%). The catalyst was filtered off and rinsed with trifluoroethanol. The filtrate and wash solution were brought to dryness and the combined residue was chromatographed over silica gel in chloroform/methanol/water, whereby 0.1.8 g 5-(L-alanylaminomethyl)-3,6-dimethoxy-9,9-dimethylxanthene-4-acetic acid was obtained as a colourless foam; IR 3450-2400, 1679, 1606, 1575, 1493 cm-1.
Workup
- filtrationThe catalyst was filtered off
- washrinsed with trifluoroethanol
- washThe filtrate and wash solution
- customthe combined residue was chromatographed over silica gel in chloroform/methanol/water
Sources & evidence
- ORD record
- ord-d3743ab01f3848f282574fb056385ec2
- Source dataset
- uspto-grants-1998_09
- Patent number
- US05811548
Reaction notes
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