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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243374Generated: October 30, 2026

1-Methylpiperazine → HCID 178463571, compound

https://huagongshe.com/reaction/243374

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant5-Fluoro-3-phenyl-2-{(S)-1-[9-(tetrahydropyran-2-yl)-9H-purin-6-ylamino]ethyl}-3H-benzoimidazole-4-carboxylic acidHCID 68157461—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductAmmonium HydroxideHCID 14923—
ProductHCID 178463571HCID 178463571118.1%

Reaction Steps

A mixture of 5-fluoro-3-phenyl-2-{(S)-1-[9-(tetrahydropyran-2-yl)-9H-purin-6-ylamino]ethyl}-3H-benzoimidazole-4-carboxylic acid (100 mg, 0.2 mmol), HATU (91 mg, 0.24 mmol), 1-methylpiperazine (33 μL, 0.3 mmol) and DIPEA (69 μL, 0.4 mmol) in DCM (2 mL) was stirred at RT for 1 h. The crude mixture was diluted with water and extracted with DCM. The aqueous phase was further extracted with DCM and the combined organic fractions were dried (MgSO4) and concentrated in vacuo. The resulting residue was dissolved in MeOH (1 mL) and 4N HCl in dioxane (0.25 mL) and the mixture stirred at RT for 30 min. The volatiles were removed under reduced pressure and the resulting residue purified by HPLC (Waters C18 XBridge, on a 20 min gradient 10-90%, 0.1% NH4OH in acetonitrile/water) to afford 202 (59 mg, 59%). LCMS (Method K): RT 2.02 min [M+H]+ 500.1. 1H NMR (DMSO-d6+TFA-D, 400 MHz, 80° C.): δ 12.45 (1H, s), 8.52 (1H, br s), 8.44 (1H, d, J=6.07 Hz), 7.85-7.80 (1H, m), 7.56-7.27 (5H, m), 7.24-7.17 (1H, m), 5.67 (1H, br s), 3.76-3.52 (1H, m), 3.49-3.37 (1H, m), 3.34-2.87 (7H, m), 2.81 (3H, s), 1.71-1.64 (3H, m)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653089B2
Source datasetuspto-grants-2014_02
ORD IDord-9fd62289fce34fff8916b5e60a91eca1
Source noteuspto-grants-2014_02