Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943429Generated: November 2, 2026

Water → HCID 178474335, compound

https://huagongshe.com/reaction/1943429

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHCID 59624715HCID 59624715—
ReactantHCID 178511674HCID 178511674—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 178474335HCID 17847433526.7%

Reaction Steps

A solution of 6-chloro-N-(3-fluoropyridin-4-yl)-8-(N-(4-methoxybenzyl)acetamido)imidazo[1,2-b]pyridazine-3-carboxamide 19B (30 mg, 0.064 mmol) and trans-cyclohexane-1,4-diamine (14.61 mg, 0.128 mmol) in NMP (0.5 mL) was heated at 70° C. for 2.5 h, and then cooled to room temperature. Water was added. The mixture was extracted with EtOAc for three times, the combined extracts were washed with H2O and brine, and then concentrated. The resulting residue was treated with MeOH. The solid was filtered off, and the filtrate was purified by preparative HPLC. The desired fraction was concentrated to dryness and then dissolved in TFA (1 mL). The solution was stirred at 70° C. for 6 h and then concentrated. The residue was treated with MeOH/DCM, and concentrated again to give a solid, which was triturated with ether. The solid was collected by filtration, rinsed with ether, and dried under vacuum to give 19C (7.3 mg, 21%) as an off white solid. [M+H]=427. HPLC Peak Rt=2.018 minutes. (Chromolith column 4.6×50 mm eluting with 10-90% aqueous methanol over 4 minutes containing 0.1% TFA, 4 mL/min, monitoring at 220 nm.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389527B2
Source datasetuspto-grants-2013_03
ORD IDord-e4cb89336b08403cac3c3f5daba8015b
Source noteuspto-grants-2013_03