Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclopentene | HCID 8882 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | HCID 22676791 | HCID 22676791 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 22676838 | HCID 22676838 | 45% |
Reaction Steps
Cyclopentene (0.44 mL, 341 mg, 5.0 mmol), palladium acetate (22 mg, 0.10 mmol), tetrabutylammonium bromide (322 mg, 1.0 mmol) and potassium acetate (295 mg, 1.0 mmol) were added to a stirred solution of ethyl 3-(4-tert-butylphenyl)-1-(3-methoxybenzyl)-5-{[(trifluoromethyl)sulfonyl]oxy}-1H-indole-2-carboxylate (Example 125, 570 mg, 1.0 mmol) in N,N-dimethylformamide (5 mL). The reaction was stirred for 48 h and then diluted with ethyl acetate (100 mL). The solution was washed with brine, dried over anhydrous magnesium sulfate, and concentrated in vacuo. Flash chromatography of the residue over silica gel using 6:1 ethyl acetate/hexane gave 230 mg, (45%) of the desired product. The product had: 1H NMR (300 MHz, acetone-D6) δ 7.49-7.56 (m, 3 H), 7.37-7.43 (m, 3 H), 7.17-7.23 (m, 2 H), 6.68-6.92 (m, 3 H), 4.09 (q, 3 H), 3.92-4.01 (m, 1 H), 3.75 (s, 3 H), 2.31-2.50 (m, 3 H), 1.62-1.77 (m, 1 H), 1.39 (s, 9 H), 0.98 (t, 3 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06787651B2 |
|---|
| Source dataset | uspto-grants-2004_09 |
|---|
| ORD ID | ord-beb3c39e352b4fbb9fd71146daa41474 |
|---|
| Source note | uspto-grants-2004_09 |
|---|