Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Reactant | 1-(2-Chloroethyl)pyrrolidine hydrochloride | HCID 81668 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (7-Chlorothieno[3,2-b]pyridin-2-yl)methanol | HCID 22143534 | — |
| Catalyst | Benzyltriethylammonium bromide | HCID 165294 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 22143516 | HCID 22143516 | 71.1% |
Reaction Steps
A mixture of 2-(hydroxymethyl)-7-chlorothieno[3,2-b]pyridine 114a (0.35 g, 1.8 mmole), 1-(2-chloro-ethyl)-pyrrolidine hydrochloride (31 g, 18 mmole), benzyltriethylammonium bromide (0.2 g, 0.7 mmole) and 19 M sodium hydroxide (10 mL) in toluene was refluxed for three hours. The reaction mixture was buffered with 50% saturated sodium bicarbonate and the workup was performed with ethyl acetate, brine and magnesium sulfate. The crude product was purified over silica gel (100 g) using 2–7% methanol-chloroform with 0.1% ammonium hydroxide, which provided the title compound as an amber oil (0.38 g, 62%): 1H-NMR (DMSO-d6, 400 MHz) δ 8.62 (1H, d, J=5.0 Hz), 7.58 (1H, s), 7.54 (1H, d, J=5.1 Hz), 4.86 (2H, s), 3.62 (2H, t, J=6.0 Hz), 2.64 (2H, t, J=5.8 Hz), 2.49–2.47 (4H, m), 1.67–1.63 (4H, m); MS m/z 297 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07045528B2 |
|---|
| Source dataset | uspto-grants-2006_05 |
|---|
| ORD ID | ord-d0bc5a3956dd4903b5cb80c6daf814db |
|---|
| Source note | uspto-grants-2006_05 |
|---|