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HRID 1405704作成日:2026年10月27日

Tetrahydrofuran → 9-[(7-Methoxynaphthalen-2-yl)oxy]-3,4-dihydropyrido[2,1-c][1,2,4]thiadiazine 2,2-dioxide

https://huagongshe.com/reaction/1405704

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物Ethanesulfonylchloride, 2-chloro-HCID 15385—
反応物Sodium hydrideHCID 24758—
反応物3-[(7-Methoxynaphthalen-2-yl)oxy]pyridin-2-amineHCID 66748540—
溶媒WaterHCID 962—
生成物9-[(7-Methoxynaphthalen-2-yl)oxy]-3,4-dihydropyrido[2,1-c][1,2,4]thiadiazine 2,2-dioxideHCID 6674897952%

反応手順

To a mixture of sodium hydride (60%, 375 mg), 2-chloroethanesulfonyl chloride (612 mg) and dehydrated THF (15 mL) was added a mixture of 3-[(7-methoxynaphthalen-2-yl)oxy]pyridin-2-amine (500 mg) and dehydrated THF (15 mL) at room temperature. The reaction mixture was stirred for 2 hr, water was added, and THF was evaporated under reduced pressure. The resulting precipitate was washed with water and diisopropyl ether to give the title compound (348 mg) as a pale-brown solid. The obtained solid was crystallized from acetonitrile and diisopropyl ether to give a pale-brown solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08916551B2
出典データセットuspto-grants-2014_12
ORD IDord-5b416ac8cfc64e01a53921645af6ecfe
出典メモuspto-grants-2014_12