HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2-Benzyl-3-iodo-6-[(3S,4S)-3-acetoxy-4-methoxypyrrolidine-1-yl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-benzyl-3-iodo-6-[(3S,4S)-3-(3-nitrobenzenesulfonyl)oxy-4-methoxypyrrolidin-1-yl]pyridine | HCID 21058021 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2-Benzyl-3-iodo-6-[(3S,4S)-3-acetoxy-4-methoxypyrrolidine-1-yl)pyridine | HCID 131723996 | — |
Reaction Steps
4.2 ml of acetic acid was added to a mixture of 7.9 g of cesium carbonate and 15 ml of dimethyl sulfoxide. After foaming stopped, a mixture of 14.4 g of 2-benzyl-3-iodo-6-[(3S,4S)-3-(3-nitrobenzenesulfonyl)oxy-4-methoxypyrrolidine-1-yl]pyridine and 35 ml of dimethyl sulfoxide was added thereto, followed by heating under stirring for 6 hours in an oil bath kept at 70° C. in a nitrogen atmosphere. The reaction solution was cooled and then subjected to extraction with ethyl acetate-water. The organic phase was washed with water and brine brine, dried over anhydrous magnesium sulfate and then concentrated. The residue was subjected to silica gel column chromatography using 10-15% ethyl acetate/hexane, to give 7.5 g of the target compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06599917B1 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-1e6587ff034f47f3b2b7f34f4a7b2dcf |
| Source note | uspto-grants-2003_07 |