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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 529403생성일: 2026년 10월 25일

Sodium Bicarbonate → (NE,R)-N-(7-bromo-3-chlorochromeno[2,3-c]pyridin-5-ylidene)-2-methylpropane-2-sulfinamide

https://huagongshe.com/reaction/529403

반응식

참여 물질

역할이름HCID투입량
반응물Sodium BicarbonateHCID 516892—
반응물tert-Butylsulfinamide, (R)-(+)-HCID 10964479—
반응물7-Bromo-3-chloro-5H-chromeno[2,3-c]pyridin-5-oneHCID 57475636—
촉매HCID 178477244HCID 178477244—
용매TetrahydrofuranHCID 8028—
용매Sodium chloride; waterHCID 57417360—
생성물(NE,R)-N-(7-bromo-3-chlorochromeno[2,3-c]pyridin-5-ylidene)-2-methylpropane-2-sulfinamideHCID 88920351—

반응 조건

온도75 °C

반응 단계

A mixture of 7-bromo-3-chloro-5H-chromeno[2,3-c]pyridin-5-one (5.0 g, 48.3 mmol), (R)-2-methylpropane-2-sulfinamide (5.85 g, 48.3 mmol), and tetraethoxytitanium (10.00 mL, 48.3 mmol) in dry THF (100 mL) was heated at 75° C. for 24 hours. The solution was cooled to RT and slowly poured into a 2 L flask containing 0.35 L of brine and 0.35 L of saturated sodium bicarbonate. The resulting mixture was stirred vigorously for 15 minutes before being filtered through a pad of celite. The pad was washed with EtOAc. The filtrate was poured into a separatory funnel and the aqueous layer was extracted with EtOAc (2×500 mL). The combined organic layers were washed with brine, dried over sodium sulfate, filtered, and concentrated in vacuo to provide an orange solid. This solid was purified by silica gel chromatography using 0-15% Hexane/EtOAC to provide (R,E)-N-(7-bromo-3-chloro-5H-chromeno[2,3-c]pyridin-5-ylidene)-2-methylpropane-2-sulfinamide as an orange solid. [email protected] min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09346827B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-43158cf967ec4d629694d9226d79841b
출처 메모uspto-grants-2016_05