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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419374Generated: October 30, 2026

2,6-Difluoroaniline → HCID 59453010, compound

https://huagongshe.com/reaction/419374

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DifluoroanilineHCID 79647—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantHCID 59452700HCID 59452700—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59453010HCID 5945301075%

Reaction Steps

To a solution of methyl 3-[3-(2-{[2-(methyloxy)-4-(4-morpholinyl)phenyl]amino}-4-pyrimidinyl)imidazo[1,2-a]pyridin-2-yl]benzoate (65 mg, 0.12 mmol) in 2 mL THF was added 2,6-difluoroaniline (0.065 mL, 0.60 mmol) and a 1M solution of NaHMDS in THF (0.72 mL, 0.72 mmol). When LC/MS showed the reaction to be complete it was concentrated onto silica gel and purified by flash column chromatography to give 57 mg (75%) of the title compound. 1H NMR (400 MHz, DMSO-d6) δ 10.20 (s, 1H), 9.38 (s, 1H), 8.45 (s, 1H), 8.27 (s, 1H), 8.18 (d, J=5.2 Hz, 1H), 8.01 (d, J=7.6 Hz, 1H), 7.78 (d, J=7.2 Hz, 1H), 7.70 (d, J=8.8 Hz, 1H), 7.60-7.52 (m, 2H), 7.47-7.40 (m, 2H), 7.35-7.30 (m, 1H), 7.11-7.07 (m, 1H), 6.98-6.94 (m, 1H), 6.67 (s, 1H), 6.48-6.43 (m, 2H), 3.78 (s, 3H), 3.73-3.72 (m, 4H), 3.10-3.09 (m, 4H). MS (ESI) m/z=634 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093239B2
Source datasetuspto-grants-2012_01
ORD IDord-5536d3adc7394e4181133ec16dc54a0a
Source noteuspto-grants-2012_01