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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233115Generated: October 30, 2026

1-Propanol, 3-amino-2,2-dimethyl- → 3-{4-[2-(4-Fluorophenyl)-8-isopropoxyimidazo[1,2-a]pyrazin-3-yl]-pyrimidin-2-ylamino}-2,2-dimethylpropan-1-ol

https://huagongshe.com/reaction/2233115

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Propanol, 3-amino-2,2-dimethyl-HCID 117326—
Reactant2-(4-Fluorophenyl)-8-isopropoxy-3-(2-methanesulfonylpyrimidin-4-yl)-imidazo[1,2-a]pyrazineHCID 58869538—
SolventAcetonitrileHCID 6342—
Product3-{4-[2-(4-Fluorophenyl)-8-isopropoxyimidazo[1,2-a]pyrazin-3-yl]-pyrimidin-2-ylamino}-2,2-dimethylpropan-1-olHCID 1605045165.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

A suspension of 2-(4-fluorophenyl)-8-isopropoxy-3-(2-methanesulfonylpyrimidin-4-yl)-imidazo[1,2-a]pyrazine (0.16 g, 0.37 mmol) and 3-amino-2,2-dimethylpropan-1-ol (TCI-US, 0.208 g, 0.74 mmol) in ACN (5 mL) was heated at about 80° C. overnight to give a clear solution. The reaction mixture was cooled to ambient temperature, the volatiles were evaporated, and the resulting residue was dissolved in DCM and washed with water. The organic phase was dried over MgSO4, filtered, and evaporated to give a white solid that was triturated with heptane to afford 0.109 g (64.7%) the title compound as a white solid: LC/MS (Table 1, Method g) Rt=3.01 min; MS m/z: 494.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709468B2
Source datasetuspto-grants-2010_05
ORD IDord-ae0c9fe3293e4b8db6d421c13d94dfb3
Source noteuspto-grants-2010_05