Ethanol → HCID 67451161, compound
Reaction equation
[CH3:1][C:2]1[O:6][C:5]([C:7]([NH:9][C:10]([C:13]2[N:19]([CH3:20])[C:17](=[O:18])[C:16]([OH:21])=[C:15]([C:22]([NH:24][CH2:25][C:26]3[CH:27]=[CH:28][C:29]([F:32])=[CH:30][CH:31]=3)=[O:23])[N:14]=2)([CH3:12])[CH3:11])=[O:8])=[N:4][N:3]=1.C(O)C.C(#N)C.C([O-])(=O)C.[Ca+2:43].C([O-])(=O)C>C1CCCCC1.O>[CH3:1][C:2]1[O:6][C:5]([C:7]([NH:9][C:10]([C:13]2[N:19]([CH3:20])[C:17](=[O:18])[C:16]([OH:21])=[C:15]([C:22]([NH:24][CH2:25][C:26]3[CH:27]=[CH:28][C:29]([F:32])=[CH:30][CH:31]=3)=[O:23])[N:14]=2)([CH3:12])[CH3:11])=[O:8])=[N:4][N:3]=1.[Ca:43]Participants
7
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 67.5 °C
Procedure
Raltegravir (10 gm), ethanol (60 ml), acetonitrile (40 ml), water (2 ml) and calcium acetate (4 gm) were added at 25 to 30° C. The contents were heated to 65 to 70° C. and distilled off solvent completely under vacuum at 45° C. to obtain residue. To the residue was added cyclohexane (50 ml) and again distilled to obtain residue. Cyclohexane (100 ml) was added to the residue and stirred for 5 hours at room temperature. The solid obtained was collected by filtration and dried to obtain 10 gm of raltegravir calcium.
Workup
- distillationdistilled off solvent completely under vacuum at 45° C.
- customto obtain residue
- distillationagain distilled
- customto obtain residue
- customThe solid obtained
- filtrationwas collected by filtration
- customdried
Sources & evidence
- ORD record
- ord-61d5965243194960a80bd317e0495269
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08962833B2
Reaction notes
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