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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377907Generated: October 30, 2026

2-(Di-tert-butylphosphino)biphenyl → HCID 59856805, compound

https://huagongshe.com/reaction/2377907

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Di-tert-butylphosphino)biphenylHCID 2734215—
Reactant4-(6-Chloro-5-methyl-pyrimidin-4-yloxy)-piperidine-1-carboxylic acid isopropyl esterHCID 11493357—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 67202441HCID 67202441—
Catalystpalladium(II) acetateHCID 167845—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 59856805HCID 5985680530.1%

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of 4-amino-3-fluoro-N-(2-isopropoxy-ethyl)-benzenesulfonamide (116 mg, 0.42 mmol), 4-(6-chloro-5-methyl-pyrimidin-4-yloxy)-piperidine-1-carboxylic acid isopropyl ester (100 mg, 0.3 mmol), palladium acetate (3 mg, 0.017 mmol), biphenyl-2-yl-di-tert-butyl-phosphane (7.1 mg, 0.034 mmol), and sodium t-butoxide (87 mg, 0.90 mmol) in dioxane (2 mL) was heated under microwave irradiation for 60 min at 150° C. The crude mixture was concentrated in vacuo and purified by HPLC to provide Compound A106 as a brown solid (50 mg, 22%). 1H NMR (CDCl3, 400 MHz) δ 1.04 (d, 6H), 1.19 (d, 6H), 1.67-1.78 (m, 2H), 1.89-1.99 (m, 5H), 3.05 (t, 2H), 3.30-3.40 (m, 4H), 3.42-3.52 (m, 1H), 3.66-3.76 (m, 1H), 4.87 (h, 1H), 5.19-5.38 (m, 2H), 7.58 (t, 3H), 7.90-7.98 (s broad, 1H), 8.24 (t, 1H), 8.35 (s, 1H). Exact mass calculated for C23H36FN5O6S 553.65, found 554.6 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07470699B2
Source datasetuspto-grants-2008_12
ORD IDord-dc23e022521148ab892fd9767ffc8c31
Source noteuspto-grants-2008_12