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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605939Generated: October 29, 2026

Dabco → HCID 57590026, compound

https://huagongshe.com/reaction/605939

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDabcoHCID 9237—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Fluoro-4-(4-morpholinyl)benzenamineHCID 11481003—
Reactant5,8-Dibromo-(1,2,4)triazolo(1,5-a)pyrazineHCID 49758022—
Reactant4-{8-[4-(4-Methyl-piperazin-1-yl)-phenylamino]-[1,2,4]triazolo[1,5-a]pyrazin-5-yl}-thiophene-2-carboxylic acid amideHCID 57589928—
SolventIsopropanolHCID 3776—
ProductHCID 57590026HCID 57590026—

Reaction Steps

This compound may be prepared using methods as described for Compound 6, step 1, using 5,8-dibromo-[1,2,4]triazolo[1,5-a]pyrazine (0.105 g, 0.89 mmol), 2-fluoro-4-morpholin-4-yl-phenylamine (93 mg, 0.474 mmol), DIPEA (0.123 mL, 0.706 mmol) and 1,4-diazabicyclo[2.2.2]octane (53 mg, 0.472 mmol) in 2-propanol (2 mL). The reaction mixture is partitioned between DCM and 10% citric acid (aq) solution, the organic layer is separated and washed with 10% citric acid solution, water and brine, dried over MgSO4, filtered and concentrated in vacuo. The title compound is isolated as a pale red solid (77 mg, 42%) and used in the next step without further purification. LCMS: Rt 3.48 min (89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915256B2
Source datasetuspto-grants-2011_03
ORD IDord-af2cd5354d964a8d8dcb7ea659889451
Source noteuspto-grants-2011_03