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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233110Generated: October 30, 2026

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

https://huagongshe.com/reaction/2233110

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Propanol, 3-amino-2,2-dimethyl-HCID 117326—
Reactant2-(2,4-Difluorophenyl)-3-(2-methanesulfonylpyrimidin-4-yl)-8-methylimidazo[1,2-a]pyrazineHCID 57438774—
SolventAcetonitrileHCID 6342—
Product3-{4-[2-(2,4-Difluorophenyl)-8-methylimidazo[1,2-a]pyrazin-3-yl]-pyrimidin-2-ylamino}-2,2-dimethylpropan-1-olHCID 1605045059.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of 2-(2,4-difluorophenyl)-3-(2-methanesulfonylpyrimidin-4-yl)-8-methyl-imidazo[1,2-a]pyrazine (1.4 g, 3.5 mmol) in ACN (30 mL) was added 3-amino-2,2-dimethyl-propan-1-ol (Lancaster, 0.79 g, 7.7 mmol). The mixture was heated to about 80° C. After about 16 h, the mixture was treated with additional 3-amino-2,2-dimethyl-propan-1-ol (Lancaster, 0.20 g, 1.9 mmol) and heated at about 80° C. for about another 4 h. The mixture was filtered through a pad of silica gel and eluted with EtOAc. The solution was evaporated, triturated with ether, and then filtered. The solid was dissolved in hot methanol (˜10 mL). The solution was cooled and the solvent evaporated. The resulting solid was dried at 100° C. under vacuum to yield the title compound as a white solid (0.88 g, 59%): LC/MS (Table 1, Method g) Rt=2.38 min; MS m/z: 425.2 (M+H)+, mp 173.8-174.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709468B2
Source datasetuspto-grants-2010_05
ORD IDord-7423c8573e034e4fa5c4cbf88487ce33
Source noteuspto-grants-2010_05