Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374431Generated: October 30, 2026

Sodium hexamethyidisilazane → HCID 68544666, compound

https://huagongshe.com/reaction/2374431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hexamethyidisilazaneHCID 45051731—
Reactant2H-[1,3]Dioxolo[4,5-b]pyridin-7-amineHCID 45079475—
Reactant4-Chloro-7-(2-chloroethoxy)-6-methoxyquinazolineHCID 59682907—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68544666HCID 6854466665.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium hexamethyldisilazane (1M solution in THF; 2 ml) was added dropwise to a mixture of 4-amino-2,3-methylenedioxypyridine (0.138 g), 4-chloro-7-(2-chloroethoxy)-6-methoxyquinazoline (0.272 g) and THF (5 ml) that had been cooled to 0° C. The mixture was stirred at 0° C. for 1 hour. The resultant mixture was allowed to warm to ambient temperature and was stirred for 2 hours. The reaction was quenched by the addition of glacial acetic acid (0.12 ml). The solvents were evaporated and the residue was partitioned between methylene chloride and an aqueous ammonium hydroxide solution. The organic layer was collected and concentrated to a small volume. Diethyl ether was added and a precipitate formed. The resultant solid was isolated, washed with diethyl ether and dried. There was thus obtained the title compound (0.245 g); NMR Spectrum: (DMSOd6) 3.97 (s, 3H), 4.04 (m, 2H), 4.45 (m, 2H), 6.12 (s, 2H), 7.13 (br d, 1H), 7.25 (s, 1H), 7.60 (d, 1H), 7.83 (s, 1H), 8.47 (s, 1H), 9.87 (br s, 1H); Mass Spectrum: M+H+ 375.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07462623B2
Source datasetuspto-grants-2008_12
ORD IDord-36a66f8376404254ab25a728b75a1e41
Source noteuspto-grants-2008_12