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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198073Generated: October 30, 2026

Tetrahydrofuran → HCID 57758058, compound

https://huagongshe.com/reaction/2198073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriacetoxyperiodinaneHCID 159087—
ReactantHCID 57758345HCID 57758345—
SolventEthyl AcetateHCID 8857—
ProductHCID 57758058HCID 5775805899.1%

Reaction Steps

To a solution of THF (5 mL) was added N-{4-[4-amino-6-(3-hydroxypropyl)pyrrolo[2,1-f][1,2,4]triazin-5-yl]phenyl}-N′-[2-fluoro-5-(trifluoromethyl)phenyl]urea (55 mg, 0.11 mmol) followed by Dess-Martin Periodinane reagent (0.29 mL, 0.14 mmol, 15% wt in CH2Cl2). The reaction was stirred until HPLC indicated completion of reaction (2 h). The reaction was diluted with EtOAc and washed with saturated aqueous NaHCO3/Na2S2O3 1:1 (3×). The aqueous layer was back extracted with EtOAc (2×). The combined organic layers were dried (Na2SO4), filtered, and evaporated to give a crude yellow solid (53 mg, 96%) that was used without further purification. 1H-NMR (DMSO-d6) δ 9.35 (s, 1H), 8.98 (s, 1H), 8.62 (d, J=7.2 Hz, 1H), 7.80 (s, 1H), 7.62 to 7.28 (m, 6H), 2.71 (t, J=7.5 Hz, 2H), 2.41 (t, J=7.4 Hz, 2H); MS [M+H]+=487; LCMS RT=2.62 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338595B2
Source datasetuspto-grants-2012_12
ORD IDord-8df23dae20804850b4f8c21f4d2eee6d
Source noteuspto-grants-2012_12