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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | tert-Butylsulfinamide, (R)-(+)- | HCID 10964479 | — |
| 반응물 | 7-Bromo-3-chloro-5H-chromeno[2,3-c]pyridin-5-one | HCID 57475636 | — |
| 촉매 | HCID 178477244 | HCID 178477244 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Sodium chloride; water | HCID 57417360 | — |
| 생성물 | (NE,R)-N-(7-bromo-3-chlorochromeno[2,3-c]pyridin-5-ylidene)-2-methylpropane-2-sulfinamide | HCID 88920351 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US09346827B2 |
|---|
| 출처 데이터셋 | uspto-grants-2016_05 |
|---|
| ORD ID | ord-43158cf967ec4d629694d9226d79841b |
|---|
| 출처 메모 | uspto-grants-2016_05 |
|---|