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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1785170Generated: October 31, 2026

Tetrahydrofuran → HCID 68884240, compound

https://huagongshe.com/reaction/1785170

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant4-Chloro-6,7-dimethoxyquinazolineHCID 2769364—
Reactant2-{[3-(7-amino-6-chloro-1,3-benzodioxol-4-yl)prop-2-yn-1-yl]oxy}-N,N-dimethylacetamideHCID 68881318—
SolventDimethylformamideHCID 6228—
SolventAmmonium ChlorideHCID 25517—
ProductHCID 68884240HCID 6888424034.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of sodium bis(trimethylsilyl)amide (1.3 ml) in tetrahydrofuran (1.0M, 1.3 mmol) was added over 5 minutes to a stirred mixture of 2-{[3-(7-amino-6-chloro-1,3-benzodioxol-4-yl)prop-2-yn-1-yl]oxy}-N,N-dimethylacetamide (0.200 g) and 4-chloro-6,7-dimethoxyquinazoline (0.132 g) in DMF (5.7 ml) cooled to 0° C. under a nitrogen atmosphere; the resultant mixture was stirred for 1.5 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 (20 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 (0.102 g). NMR Spectrum: (DMSOd6) 2.82 (s, 3H), 2.92 (s, 3H), 3.92 (s, 6H), 4.26 (s, 2H), 4.51 (s, 2H), 6.15 (s, 2H), 7.16 (s, 1H), 7.18 (s, 1H), 7.82 (s, 1H), 8.32 (s, 1H), 9.52 (s, 1H); Mass Spectrum: M+H+ 499 and 501.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504408B2
Source datasetuspto-grants-2009_03
ORD IDord-d807c194d5f2450b9a0e3beb2c146ef9
Source noteuspto-grants-2009_03