HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → (5-bromo-1H-pyrrolo[2,3-b]pyridin-3-yl)(2-chloro-3-fluoro-6-methoxyphenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 5-bromo-1H-pyrrolo[2,3-b]pyridine | HCID 10307932 | — |
| Reactant | 2-Chloro-3-fluoro-6-methoxybenzaldehyde | HCID 53407598 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (5-bromo-1H-pyrrolo[2,3-b]pyridin-3-yl)(2-chloro-3-fluoro-6-methoxyphenyl)methanol | HCID 67004061 | — |
Reaction Steps
A solution of 2-chloro-3-fluoro-6-methoxybenzaldehyde (10.55 g, 55.82 mmol), 5-bromo-7-azaindole (10.0 g, 50.76 mmol) and KOH (4.0 g, 71 mmol) in methanol (200 mL) was stirred at ambient temperature for 12 h. The reaction mixture was quenched with water and the crystallizing solid was filtered and dried to give the title compound as a white solid. 1H NMR (DMSO-d6, 300 MHz): □ δ=3.71 (s, 3H), 5.69 (d, 1H, J=6.3 Hz), 6.55 (d, 1H, J=4.5 Hz), 7.07 (dd, 1H, J=4.5, 4.2 Hz), 7.19 (s, 1H), 7.32 (t, J=8.0 Hz), 8.30 (s, 1H), 9.60 (s, 1H), 11.38 (s, br, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08445510B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-c5bbfbb0b3f447f9887becefa6739169 |
| Source note | uspto-grants-2013_05 |