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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1785169Generated: October 31, 2026

Tetrahydrofuran → HCID 68881443, compound

https://huagongshe.com/reaction/1785169

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant4-Chloro-6,7-dimethoxyquinazolineHCID 2769364—
ReactantHCID 68882631HCID 68882631—
SolventDimethylformamideHCID 6228—
SolventAmmonium ChlorideHCID 25517—
ProductHCID 68881443HCID 6888144339.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of sodium bis(trimethylsilyl)amide (1.23 ml) in tetrahydrofuran (1.0M, 1.23 mmol) was added over 5 min. to a stirred mixture of 2-{[3-(7-amino-6-chloro-1,3-benzodioxol-4-yl)prop-2-yn-1-yl]oxy}-N-methylacetamide (0.182 g) and 4chloro-6,7-dimethoxyquinazoline (0.125 g) in DMF (6.0 ml) cooled to 0° C. under a nitrogen atmosphere; the mixture was stirred for 1.25 hr at ambient temperature. The reaction mixture was diluted with saturated aqueous ammonium chloride (60 ml) and extracted with ethyl acetate (3×30 ml). The organic extracts were washed with brine (30 ml), dried over sodium sulphate and then evaporated. The residue was purified by column chromatography on silica using increasingly polar mixtures of methanol and dichloromethane as eluent. There was thus obtained the title compound as a solid (0.106 g). NMR Spectrum: (DMSOd6) 2.62 (d, 3H), 3.91 (s, 6H), 3.98 (s, 2H), 4.50 (s, 2H), 6.15 (s, 2H), 7.15 (s, 1H), 7.17 (s, 1H), 7.76 (s, 1H), 7.80 (s, 1H), 8.31 (s, 1H), 9.52 (s, 1H); Mass Spectrum: M+H+ 485 and 487.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504408B2
Source datasetuspto-grants-2009_03
ORD IDord-08d35b9850c3446c9808c062d9860307
Source noteuspto-grants-2009_03