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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888502Generated: November 3, 2026

Sodium bis(trimethylsilyl)amide → HCID 58266623, compound

https://huagongshe.com/reaction/1888502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantHCID 58266759HCID 58266759—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58266623HCID 5826662317%

Reaction Steps

Sodium bis(trimethylsilyl)amide (3.9 mL, 3.90 mmol) was added to a solution of 5′-bromo-6′-chloro-2-fluoro-5-(4-piperidin-1-ylmethyl-phenyl)-[3,4]bipyridinyl-3′-ylamine (187 mg, 0.39 mmol) in anhydrous THF (7.0 mL) and the resultant solution stirred at ambient temperature for 20 min. The reaction mixture was diluted with water (20 mL) and extracted with DCM: MeOH (4:1, 3×20 mL). The combined organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The resultant residue was purified by flash chromatography (silica, 4 g column, ISCO, 0-15% MeOH in DCM) to afford the title compound as a beige powder (30 mg, 17%). 1H NMR (CDCl3, 400 MHz): 9.17 (d, J=2.0 Hz, 1H), 8.86 (d, J=2.0 Hz, 1H), 8.67 (s, 1H), 7.65 (d, J=7.5 Hz, 2H), 7.49 (d, J=7.5 Hz, 2H), 3.59 (s, 2H), 2.51-2.47 (m, 4H), 1.68-1.59 (m, 4H), 1.51-1.45 (m, 2H). LCMS (Method A): RT=7.10 min, M+H+=455/457.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501765B2
Source datasetuspto-grants-2013_08
ORD IDord-613b196142e5494b9dcc8c7ff828803d
Source noteuspto-grants-2013_08