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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 513312Generated: October 30, 2026

Trifluoroacetic acid → HCID 67502054, compound

https://huagongshe.com/reaction/513312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
Reactant4-(2,3-Difluorobenzylamino)-6-(4-(piperidin-4-yl)phenylamino)nicotinamideHCID 67500438—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 67502054HCID 67502054—

Reaction Steps

The mixture of 4-(2,3-difluorobenzylamino)-6-(4-(piperidin-4-yl)phenylamino)nicotinamide (Example 209) (80 mg, 0.17 mmol), 4-morphonlineacetic acid (100 mg, 0.68 mmol), DIEA (240 μL, 1.36 mmol) in 4 mL NMP was stirred at RT. To it was added BOP (260 mg, 0.68 mmol). The mixture was stirred at RT for overnight. To it was added TFA (0.5 mL). The mixture was subjected to reverse phase preparative HPLC to isolate the title compound (70 mg). MS found for C31H36F2N6O2 as (M+H)+ 563.5. UV: λ=259 nm. 1H NMR: (CD3OD) δ 8.18 (1H, s), 7.34-7.11 (7H, m), 5.80 (1H, s), 4.55 (2H, s), 4.35-4.26 (4H, m), 3.83 (2H, m), 3.60 (2H, m), 3.05 (2H, m), 2.89 (1H, m), 1.95-1.57 (10H, m) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102625B2
Source datasetuspto-grants-2015_08
ORD IDord-1de118e970aa44fbb081c79dd9a0acd2
Source noteuspto-grants-2015_08