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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411594Generated: October 31, 2026

1-Amino-4-methylpiperazine → HCID 178440269, compound

https://huagongshe.com/reaction/411594

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Amino-4-methylpiperazineHCID 81349—
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
ReactantHCID 178440270HCID 178440270—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178440269HCID 17844026958%

Reaction Conditions

Temperature45 °C

Reaction Steps

Part F: To a stirred solution of 49 mg (0.10 mmol) of 1-(2,4,6-trichlorophenyl)-3-isopropyl-6-(4-(carboxy)benzyl)pyrazolo[3,4-d]pyrimidin-4-one and 0.06 mL(0.5 mmol) of 1-amino-4-methylpiperazine in 1 mL of DMF was added 0.052 mL of DIEA followed by 48 mg (0.15 mmol) of TBTU. The solution was stirred 16 h at 45° C., cooled to RT, and poured into water. The mixture was extracted with EtOAc, and the organic extract was concentrated under reduced pressure. Chromatography with 4:1 chloroform-MeOH afforded 34 mg (58%) of 1-(2,4,6-trichlorophenyl)-3-isopropyl-6-(4-(4-methylpiperazin-1-ylaminocarbonyl)benzyl)pyrazolo[3,4-d]pyrimidin-4-on as a white solid. Mass spec: (ESI+) 588(M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06559152B2
Source datasetuspto-grants-2003_05
ORD IDord-3963827ae62441e2a0021cd4c101b0c5
Source noteuspto-grants-2003_05