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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243375Generated: October 30, 2026

Morpholine → HCID 178463572, compound

https://huagongshe.com/reaction/243375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
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 178463572HCID 178463572141.8%

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), morpholine (26 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 (2 mL) and 4N HCl in dioxane (0.25 mL) and the mixture was 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 203 (69 mg, 71%). LCMS (Method K): RT 2.64 and 2.67 min [M+H]+ 487.1. 1H NMR (DMSO-d6+TFA-D, 400 MHz, 80° C.): δ 8.52 (1H, br s), 8.46 (1H, d, J=6.25 Hz), 7.83-7.75 (1H, m), 7.57-7.43 (5H, m), 7.32-7.15 (2H, m), 5.66 (1H, br s), 3.50-3.24 (5H, m), 3.15-3.05 (1H, m), 3.04-2.95 (1H, m), 2.70-2.58 (1H, m), 1.74-1.65 (3H, m)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653089B2
Source datasetuspto-grants-2014_02
ORD IDord-5f0244e304cd4478a54f5c3b1dadd80f
Source noteuspto-grants-2014_02