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HRID 1748008作成日:2026年10月26日

Ethanesulfonylchloride, 2-chloro- → 9-(4-((Tert-butyl(dimethyl)silyl)oxy)phenyl)-3,4-dihydropyrido[2,1-c][1,2,4]thiadiazine 2,2-dioxide

https://huagongshe.com/reaction/1748008

反応式

関与物質

役割名称HCID仕込み量
反応物Ethanesulfonylchloride, 2-chloro-HCID 15385—
反応物Sodium hydrideHCID 24758—
反応物3-(4-((Tert-butyl(dimethyl)silyl)oxy)phenyl)pyridin-2-amineHCID 66747707—
溶媒TetrahydrofuranHCID 8028—
生成物9-(4-((Tert-butyl(dimethyl)silyl)oxy)phenyl)-3,4-dihydropyrido[2,1-c][1,2,4]thiadiazine 2,2-dioxideHCID 66747725—

反応手順

To a suspension of NaH (60%, 42.0 g) in THF (dry) (350 mL) was added 2-chloroethanesulfonyl chloride (44.5 mL) at 0° C. and the mixture was stirred for 10 min at the same temperature. A solution of 3-(4-((tert-butyl(dimethyl)silyl)oxy)phenyl)pyridin-2-amine (78.8 g) in THF (dry) (350 mL) was added at 0° C. and the mixture was stirred at room temperature under N2 overnight. The mixture was quenched with water at 0° C. carefully. Additional water was added to form precipitates which were washed with water and EtOAc and collected to give the title compound (65.5 g) as an off-white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09150591B2
出典データセットuspto-grants-2015_10
ORD IDord-578e488008ca4f13bebbaf74e9cc7000
出典メモuspto-grants-2015_10