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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377751Generated: October 29, 2026

Tributyl(prop-1-yn-1-yl)stannane → HCID 11256520, compound

https://huagongshe.com/reaction/2377751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyl(prop-1-yn-1-yl)stannaneHCID 2733165—
ReactantHCID 11246214HCID 11246214—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 11256520HCID 1125652076.1%

Reaction Conditions

Temperature96 °C

Reaction Steps

2-[2-(3-(R)-Amino-piperidin-1-yl)-5-bromo-6-oxo-6H-pyrimidin-1-ylmethyl]-benzonitrile (Example 1) (120 mg, 0.31 mmol) and tributyl(1-propynyl)tin (140 μL, 0.46 mmol) were stirred in dioxane (5 mL) in a flask purged with nitrogen. Tetrakis(triphenylphosphine)palladium(0) (54 mg, 0.046 mmol) was added, and the solution stirred at 96° C. for 40 h. Concentration in vacuo and purification by silica gel chromatography (16% MeOH/CHCl3) gave 82 mg (76%) of the title compound as a clear oil. 1H NMR (400 MHz, MeOD-d4): δ 7.82 (s, 1H), 7.64 (d, 1H, 7.6 Hz), 7.53 (t, 1H, J=7.6 Hz), 7.36 (t, 1H, J=7.6 Hz), 7.16 (d, 1H, J=7.6 Hz), 5.30 (s, 2H), 3.40-3.48 (m, 1H), 3.21-3.30 (m, 1H), 2.78-2.89 (m, 2H), 2.58-2.66 (m, 1H), 1.91 (s, 3H), 1.85-1.93 (m, 1H), 1.52-1.74 (m, 2H), 1.18-1.27 (m, 1H). MS (ES) [m+H] calc'd for C20H21N5O, 348; found 348.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07470700B2
Source datasetuspto-grants-2008_12
ORD IDord-a33b610ada724811909bcb519f42a677
Source noteuspto-grants-2008_12