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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1785168Generated: November 2, 2026

Tetrahydrofuran → HCID 68884085, compound

https://huagongshe.com/reaction/1785168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant4-Chloro-6,7-dimethoxyquinazolineHCID 2769364—
ReactantHCID 68881408HCID 68881408—
SolventDimethylformamideHCID 6228—
SolventAmmonium ChlorideHCID 25517—
ProductHCID 68884085HCID 6888408550.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of sodium bis(trimethylsilyl)amide (1.5 ml) in tetrahydrofuran (1.0M, 1.5 mmol) was added over 5 min. to a stirred mixture of 4-(7-amino-6-chloro-1,3-benzodioxol-4yl)-2-methylbut-3-yn-2-ol (0.186 g) and 4-chloro-6,7-dimethoxyquinazoline (0.150 g) in DMF (6.5 ml) cooled to 0° C. under a nitrogen atmosphere. The mixture was stirred for 1 hr at ambient temperature. The reaction mixture was diluted with saturated aqueous ammonium chloride (70 ml) and extracted with ethyl acetate (3×30 ml). The organic extracts were washed with brine (20 ml), dried over sodium sulphate and then evaporated. The residue was purified by column chromatography on silica using increasingly polar mixtures of ethyl acetate and isohexane as eluent. There was thus obtained the title compound as a solid (0.150 g). NMR Spectrum: (DMSOd6) 1.47 (s, 6H), 3.90 (s, 3H), 3.91 (s, 3H), 5.50 (s, 1H), 6.13 (s, 2H), 7.04 (s, 1H), 7.17 (s, 1H), 7.80 (s, 1H), 8.31 (s, 1H), 9.48 (s, 1H); Mass Spectrum: M+H+ 442 and 444.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504408B2
Source datasetuspto-grants-2009_03
ORD IDord-7f3d20b3e59140b39dfe448353bd2730
Source noteuspto-grants-2009_03