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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantDichloromethaneHCID 6344—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178524810HCID 178524810—
Product4-Chloro-6-fluoropyrrolo[1,2-b]pyridazine-3-carboxamideHCID 6829246681%

Reaction Conditions

Temperature120 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221826B2
Source datasetuspto-grants-2015_12
ORD IDord-27c6e7323a4240209cf4b7d37b4aad24
Source noteuspto-grants-2015_12