HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374431Generated: October 30, 2026
Sodium hexamethyidisilazane → HCID 68544666, compound
https://huagongshe.com/reaction/2374431
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hexamethyidisilazane | HCID 45051731 | — |
| Reactant | 2H-[1,3]Dioxolo[4,5-b]pyridin-7-amine | HCID 45079475 | — |
| Reactant | 4-Chloro-7-(2-chloroethoxy)-6-methoxyquinazoline | HCID 59682907 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68544666 | HCID 68544666 | 65.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07462623B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-36a66f8376404254ab25a728b75a1e41 |
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| Source note | uspto-grants-2008_12 |
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