Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | (S)-2-[3-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenylcarbamoyl]-pyrrolidine-1-carboxylic acid benzyl ester | HCID 24828649 | — |
| Reactant | HCID 62604392 | HCID 62604392 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 57977862 | HCID 57977862 | — |
Reaction Steps
A solution of (S)-2-[3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenylcarbamoyl]-pyrrolidine-1-carboxylic acid benzyl ester (74 mg, 0.16 mmol), 2-(3-bromo-phenyl)-N-cyclopropyl-acetamide (42.0 mg, 0.17 mmol), and Pd[P(Ph)3]4 (14.3 mg, 7.5 mol %) in methanol (2 mL), NaHCO3 (sat. aq., 300 μL), and DMF (400 μL) was degassed and heated to 70° C. overnight in a sealed vial. The reaction was cooled, filtered, and purified by reverse phase HPLC to give the desired product. Yield 5.3 mg. MS: 498.2 (M+H+); H1 -NMR (DMSO-d6): δ (ppm) 0.31-0.39 (m, 2H), 0.52-0.60 (m, 2H), 1.74-2.00 (m, 3H), 2.10-2.30 (m, 1H), 2.50-2.62 (m, 1H), 3.34-3.54 (m, 2H), 4.28-4.38 (m, 1H), 4.85-5.08 (m, 2H), 6.95-7.55 (m, 12H), 7.80-7.92 (m, 1H), 8.05-8.18 (m, 1H), 10.05-10.12 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07629340B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-f0ccad77ed304a7aac9595d8ce63e299 |
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| Source note | uspto-grants-2009_12 |
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