Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175983Generated: October 31, 2026

2-(Tri-n-butylstannyl)oxazole → HCID 90413092, compound

https://huagongshe.com/reaction/2175983

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Tri-n-butylstannyl)oxazoleHCID 15486183—
ReactantHCID 90412891HCID 90412891—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 90413092HCID 9041309272%

Reaction Conditions

Temperature145 °C

Reaction Steps

In a microwave vial was dissolved the title compound of Example 277 (30 mg, 0.06 mmol) and 2-(tributylstannyl)oxazole (15 μL, 0.07 mmol) in DME (1 mL). The solution was degassed with N2 for 5 minutes then CuI (1 mg, 0.0045 mmol) and Pd(PPh3)4 (5 mg, 0.0045 mmol) were added. The reaction was purged with N2 and heated at 145° C. for 3 h. The reaction was cooled to rt, filtered through a pad of celite and purified via prep HPLC to give the title compound (19 mg, 72%). MS (ESI) mass calcd. for: C21H17F4N5O2, 447.1; m/z found 448.1 [M+H]+. 1H NMR (500 MHz, Chloroform-d) 8.49 (s, 1H), 8.36 (s, 0.8H), 7.85 (s, 0.8H), 7.76 (s, 0.4H), 7.62-7.45 (m, 1H), 7.43-7.33 (m, 1H), 7.32-7.23 (m, 2H), 7.23-7.09 (m, 1H), 4.91-4.85 (m, 0.4H), 4.78 (d, J=5.4 Hz, 0.6H), 4.42 (td, J=8.6, 2.8 Hz, 0.6H), 4.28 (td, J=8.2, 3.6 Hz, 0.4H), 4.00-3.95 (m, 0.6H), 3.89 (d, J=4.4 Hz, 0.4H), 2.23-1.44 (m, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062078B2
Source datasetuspto-grants-2015_06
ORD IDord-5ac7fcc6e8e14cfe95a160b8c7ae12e2
Source noteuspto-grants-2015_06