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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796660Generated: October 27, 2026

Water → 3-cyano-5-methyl-4-(4-phenoxy-phenylamino)-pyrrolo[1,2-b]pyridazin-6-carbonyl-N-hydroxylmorpholinyl-acetamidine

https://huagongshe.com/reaction/1796660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Cyano-5-methyl-4-(4-phenoxy-phenylamino)-pyrrolo[1,2-b]pyridazine-6-carbonyl chlorideHCID 22179609—
ReactantHCID 178513433HCID 178513433—
SolventDimethylformamideHCID 6228—
Product3-cyano-5-methyl-4-(4-phenoxy-phenylamino)-pyrrolo[1,2-b]pyridazin-6-carbonyl-N-hydroxylmorpholinyl-acetamidineHCID 178429086—

Reaction Steps

To a solution of N-hydroxy-morpholine-4-carboxamidine (Example 419A) (20.2 mg, 0.13 mmol) and Hunig's base (45 μl, 0.26 mmol) in DMF (1 ml) at −5° C. was added a solution of 3-cyano-5-methyl-4-(4-phenoxy-phenylamino)-pyrrolo[1,2-b]pyridazine-6-carbonyl chloride (Example 412B) (51 mg, 0.12 mmol) in DMF (1 ml) via syringe. The reaction mixture was warmed to rt, after 20 min, diluted with EtOAc, poured into water (50 ml), extracted with EtOAc (2×50 ml). The combined extracts were dried with Na2SO4, concentrated in vacuo and purified by prep. TLC to give the title compound (23 mg, 37%) (5% MeOH—CHCl3). It has a retention time of 5.79 min (standard LC1 method, 8 min run). LCMS Found: (M+H)+=512.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07030112B2
Source datasetuspto-grants-2006_04
ORD IDord-6a20af5a3092424689cd646fc8512e16
Source noteuspto-grants-2006_04