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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016424Generated: November 1, 2026

2-(Tributylstannyl)furan → HCID 18406842, compound

https://huagongshe.com/reaction/1016424

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Tributylstannyl)furanHCID 4393688—
ReactantHCID 18406952HCID 18406952—
ProductHCID 18406842HCID 1840684259%

Reaction Steps

This was prepared in 59% yield using a similar procedure to that described in Example 53 except using 2-(tributylstannyl)furan instead of 2-(tributylstannyl)pyridine and 3-bromo-2-(2-ethyl-2H-[1,2,4]triazol-3-ylmethoxy)-7-(2-fluorophenyl)pyrazolo[1,5-d][1,2,4]triazine instead of 3-bromo-7-(2-fluorophenyl)-2-(2-methyl-2H-[1,2,4]triazol-3-ylmethoxy)-pyrazolo[1,5-d][1,2,4]triazine. Data for title compound: mp=182-183° C. (CH2Cl2-EtOAc); 1H NMR (360 MHz, CDCl3) δ 1.39 (3H, t, J=7.3 Hz), 4.17 (2H, q, J=7.3 Hz), 5.59 (2H, s), 6.51 (1H, m), 6.70 (1H, m), 7.28 (1H, m), 7.39 (1H, dt, J=7.6 and 0.9 Hz), 7.56 (1H, m), 7.65 (1H, m), 7.81 (1H, m), 7.90 (1H, s), 9.69 (1H, s); MS (ES+) m/e 406 [MH]+; Anal. Found C, 58.57; H, 4.08; N, 23.87%. C20H16FN7O2.0.3H2O requires C, 58.48; H, 4.07; N, 23.87%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06476030B1
Source datasetuspto-grants-2002_11
ORD IDord-c5c30e6109eb495b986c8f3eed263116
Source noteuspto-grants-2002_11