Isopropyl iodide → Latanoprost
Reaction equation
[CH3:1][CH:2]([O:4][C:5]([CH2:7][CH2:8][CH2:9]/[CH:10]=[CH:11]\[CH2:12][C@@H:13]1[C@@H:17]([CH2:18][CH2:19][C@@H:20]([OH:29])[CH2:21][CH2:22][C:23]2[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=2)[C@H:16]([OH:30])[CH2:15][C@@H:14]1[OH:31])=[O:6])[CH3:3].N[C@H](C(O)=O)CCCNC(=N)N.C(I)(C)C.C([O-])(=O)C.[NH4+].C(OCC)(=O)C>CO.O>[CH3:3][CH:2]([O:4][C:5]([CH2:7][CH2:8][CH2:9]/[CH:10]=[CH:11]\[CH2:12][C@@H:13]1[C@@H:17]([CH2:18][CH2:19][C@@H:20]([OH:29])[CH2:21][CH2:22][C:23]2[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=2)[C@H:16]([OH:30])[CH2:15][C@@H:14]1[OH:31])=[O:6])[CH3:1]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
To 1.0 gram of Latanoprost L-arginine salt (2) in MeOH/H2O (4:1, 20 mL) is added 2.01 equivalents of isopropyl iodide (99%, Cat #148938, Sigma-Aldrich, St. Louis, Mo.). and the solution is stirred overnight. Saturated aqueous ammonium acetate is added along with ethyl acetate and the layers are separated. The organic layer is separated, and the solvents removed in vaccuo, and the material is chromatographed to give latanoprost as the isopropyl ester (6).
Workup
- customthe layers are separated
- customThe organic layer is separated
- customthe solvents removed in vaccuo
- customthe material is chromatographed
Sources & evidence
- ORD record
- ord-7a6f23ae833f4666a1bb459dba1610f3
- Source dataset
- uspto-grants-2014_05
- Patent number
- US08722739B2
Reaction notes
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