HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-Ethyl-1-(4-fluoro-benzyl)-1H-pyrrolo[2,3-c]pyridine-5-carboxylic acid hydroxyamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hydroxylamine | HCID 787 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1h-Pyrrolo[2,3-c]pyridine-5-carboxylic acid,4-ethyl-1-[(4-fluorophenyl)methyl]-,ethyl ester | HCID 59855822 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Ethyl-1-(4-fluoro-benzyl)-1H-pyrrolo[2,3-c]pyridine-5-carboxylic acid hydroxyamide | HCID 11493352 | — |
Reaction Steps
To a solution of 4-ethyl-1-(4-fluoro-benzyl)-1H-pyrrolo[2,3-c]pyridine-5-carboxylic acid ethyl ester (57 mg, 0.175 mmol) in EtOH (2 mL), was added a 10% wt/wt solution of NaOH in water (0.5 mL) and a 50% wt/wt solution of hydroxylamine in water (1 mL). The reaction was stirred at room temperature for 18 hours, and then 1 N HCl was added till a pH of 7 was reached. The reaction was concentrated by rotary evaporation, and then purified by preparative HPLC to give the desired product. Yield 10 mg, 18%. 1H NMR (400 MHz, CDCl3) δ 1.36 (t, J=7.58 Hz, 3H), 3.47 (q, J=7.41 Hz, 2H), 5.38 (s, 2H), 6375 (d, J=3.28 Hz, 1H), 7.02 (m, 2H), 7.13 (m, 2H), 7.30 (m, 1H), 8.43 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07468375B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-88601713bd6a4d08a3209b90ad6b0f10 |
| Source note | uspto-grants-2008_12 |