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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 229621Generated: October 28, 2026

Tetrahydrofuran → HCID 57758345, compound

https://huagongshe.com/reaction/229621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantHCID 57758336HCID 57758336—
SolventEthyl AcetateHCID 8857—
ProductHCID 57758345HCID 5775834598%

Reaction Steps

To a solution of THF (6 mL) was added ethyl 3-(4-amino-5-{4-[({[2-fluoro-5-(trifluoromethyl)phenyl]amino }carbonyl)amino]phenyl}pyrrolo[2,1-f][1,2,4]triazin-6-yl)propanoate (62 mg, 0.12 mmol) followed by DIBAL (0.6 mL, 0.6 mmol, 1.0M solution in toluene). The reaction was stirred at rt for 1 h. Additional DIBAL (1.2 mL, 1.2 mmol, 1.0M solution in toluene) was added and stirred at rt for an additional 1 h. The reaction was diluted with EtOAc and quenched with saturated aqueous Rochelle's salt. Reaction was extracted with EtOAc (4×). The combined organic layers were dried (Na2SO4), filtered, and evaporated to dryness to afford a crude yellow solid (56 mg, 98%) that was used directly in the next step without further purification. 1H-NMR (CD3OD) δ 8.62 (d, J=7.6 Hz, 1H), 7.74 (s, 1H), 7.61 (d, J=7.6 Hz, 2H), 7.52 (s, 1H), 7.38 to 7.31 (m, 4H), 3.50 (t, J=7.1 Hz, 2H), 2.61 (t, J=7.8 Hz, 2H), 1.77 to 1.65 (m, 2H); MS [M+H]+=489; LCMS RT=2.50 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07563791B2
Source datasetuspto-grants-2009_07
ORD IDord-5f07a1653d284ac68c952030eecd9569
Source noteuspto-grants-2009_07