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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174722Generated: November 1, 2026

Sodium hydride → HCID 11397775, compound

https://huagongshe.com/reaction/1174722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
Reactant6-Chloro-N-[4-(methanesulfonyl)phenyl]-5-nitropyrimidin-4-amineHCID 21897886—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11397775HCID 1139777580.2%

Reaction Steps

4-Hydroxy-piperidine-1-carboxylic acid tert-butyl ester (3.03 mmol, 610 mg) and sodium hydride (10.6 mmol, 255 mg) were dissolved in dry THF (20 mL) and stirred for 30 minutes at room temperature. Then, (6-chloro-5-nitro-pyrimidin-4-yl)-(4-methanesulfonyl-phenyl)-amine (3.03 mmol, 1.0 g) was added. The reaction was stirred at room temperature for 30 minutes. Its progress was monitored by thin layer chromatography and LCMS. Sodium hydride was quenched with water and the desired compound was extracted in ethyl acetate. Organic solvents were evaporated in vacuo. Flash chromatography (Silica gel 60; 30/70 EtOAc/Hexanes) provided Compound A1 as a yellow solid (1.2 g, 68%). 1H NMR (400 MHz, CDCl3) δ (ppm): 10.10 (s, 1H), 8.33 (s, 1H), 7.90 (d, 2H), 7.79 (d, 2H), 5.51 (heptet, 1H), 3.58 (m, 2H), 3.46 (m, 2H), 2.97 (s, 3H), 1.84 (m, 4H), 1.36 (s, 9H). LCMS (ESI), m/z 494.4 (M+H+, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07838525B2
Source datasetuspto-grants-2010_11
ORD IDord-45db3ced7b294105903569d5c18ebf46
Source noteuspto-grants-2010_11