HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1507909Generated: October 29, 2026
Ammonia → 4-Chloro-6-fluoropyrrolo[1,2-b]pyridazine-3-carboxamide
https://huagongshe.com/reaction/1507909
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 178524810 | HCID 178524810 | — |
| Product | 4-Chloro-6-fluoropyrrolo[1,2-b]pyridazine-3-carboxamide | HCID 68292466 | 81% |
Reaction Steps
To a slurry of 6-fluoro-4-hydroxypyrrolo[1,2-b]pyridazine-3-carboxylic acid (0.400 g, 2.039 mmol) in POCl3 (15.64 g, 102 mmol) was added diisopropylethylamine (0.39 mL, 2.24 mmol) and the resulting mixture was heated at 120° C. for 3 h with stirring. The reaction was cooled to rt and concentrated to remove the excess POCl3 and the resulting residue was dissolved in dichloromethane (15 mL) and reconcentrated and the process was repeated 2 more times to afford a brown oil. This material was dissolved in dichloromethane (10 mL) and the solution was added dropwise via pipette into a 0° C. well stirred solution of ammonia in dichloromethane (˜100 mL, prepared by extracting 100 mL of conc. Aq ammonium hydroxide with 3×30 mL portions of dichloromethane). After the addition was complete, the mixture was concentrated under vacuum and water was added to give a slurry which was filtered to collect the precipitated solid. The solid was rinsed with additional water and dried to afford 355 mg (81%) of the title compound as a yellow solid. HPLC (condition B): retention time=2.05 min. LCMS (condition B): m/z 197 +ve.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09221826B2 |
|---|
| Source dataset | uspto-grants-2015_12 |
|---|
| ORD ID | ord-27c6e7323a4240209cf4b7d37b4aad24 |
|---|
| Source note | uspto-grants-2015_12 |
|---|