Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium fluoride | HCID 25953 | — |
| Reactant | 1-Iodopropane | HCID 33643 | — |
| Reactant | HCID 23508106 | HCID 23508106 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 23508126 | HCID 23508126 | — |
Reaction Steps
tert-Butyl 8-(2,4-dichlorophenyl)-6-[(triisopropylsilyl)thio]-3,4,4a,9b-tetrahydro[1]benzofuro[3,2-c]pyridine-2(1H)-carboxylate (0.111 g, 0.182 mmol) was dissolved in DMF (3 mL). 1-Iodopropane (0.2 mL) and cesium fluoride (0.060 g) were added to the reaction mixture. The reaction mixture was stirred at rt under N2 for 2.5 h. The reaction mixture was partitioned between EtOAc (30 mL) and 2:3 water:brine (25 mL). The aqueous layer was back extracted with EtOAc (30 mL). The combined organic layers were washed with water (20 mL), with brine (20 mL), dried over Na2SO4, filtered and concentrated under reduced pressure. tert-Butyl 8-(2,4-dichlorophenyl)-6-(propylthio)-3,4,4a,9b-tetrahydro[1]benzofuro[3,2-c]pyridine-2(1H)-carboxylate was obtained in quantitative yield (0.090 g). MS (ESI+) for C25H29Cl2NO3S m/z 517.0 (M+23)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06762191B2 |
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| Source dataset | uspto-grants-2004_07 |
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| ORD ID | ord-0ebebfb963184c4f800bd7b1386c5b29 |
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| Source note | uspto-grants-2004_07 |
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