Triphenylphosphine → 5-(2-Acetylthioethyl)imidazo[1,2-a]pyridine
Reaction equation
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.N(C(OC(C)C)=O)=NC(OC(C)C)=O.[N:34]1[CH:35]=[CH:36][N:37]2[C:42]([CH2:43][CH2:44]O)=[CH:41][CH:40]=[CH:39][C:38]=12.[C:46]([OH:49])(=[S:48])[CH3:47]>O1CCCC1.CN(C)C=O>[C:46]([S:48][CH2:44][CH2:43][C:42]1[N:37]2[CH:36]=[CH:35][N:34]=[C:38]2[CH:39]=[CH:40][CH:41]=1)(=[O:49])[CH3:47]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of triphenyl phosphine (4.20 g) in tetrahydrofuran (30 ml) was added dropwise, at −15° C., diisopropyl azodicarboxylate (3.16 ml). The mixture was stirred for 10 minutes at the same temperature. To the reaction mixture were, then, added a solution of 2-(imidazo[1,2-a]pyridin-5-yl)ethanol (1.00 g) in dimethylformamide (20 ml) and thioacetic acid (1.14 ml). The reaction mixture was stirred for 0.5 hour at −15° C. and, then, for 20 hours at room temperature. The reaction mixture was concentrated, which was diluted with ethyl acetate and washed with water, a saturated aqueous solution of sodium hydrogencarbonate and, then, with a saturated aqueous saline solution, followed by drying over anhydrous magnesium sulfate and concentration. The concentrate was purified by means of a column chromatography (carrier: silica gel, developing solvent: ethyl acetate-hexane, 1:1) to afford the title compound (0.52 g).
Workup
- stirringThe reaction mixture was stirred for 0.5 hour at −15° C.
- waitfor 20 hours at room temperature
- concentrationThe reaction mixture was concentrated
- additionwhich was diluted with ethyl acetate
- washwashed with water
- dry with materialby drying over anhydrous magnesium sulfate and concentration
- customThe concentrate was purified by means of a column chromatography (carrier: silica gel, developing solvent: ethyl acetate-hexane, 1:1)
Sources & evidence
- ORD record
- ord-fa1c2b09ecd84dd68e876167968e491f
- Source dataset
- uspto-grants-2001_01
- Patent number
- US06174877B1
Reaction notes
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