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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1363609생성일: 2026년 10월 25일

Triethylamine → 4-{[(2-chloro-3-nitroquinolin-4-yl)amino]methyl}tetrahydro-2H-thiopyran-4-ol

https://huagongshe.com/reaction/1363609

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2,4-Dichloro-3-nitroquinolineHCID 2785138—
반응물4-(Aminomethyl)thian-4-olHCID 45934288—
용매DichloromethaneHCID 6344—
생성물4-{[(2-chloro-3-nitroquinolin-4-yl)amino]methyl}tetrahydro-2H-thiopyran-4-olHCID 8661686559.6%

반응 단계

Under a nitrogen atmosphere triethylamine (3.91 mL, 28.0 mmol) was added to a chilled (0° C.) solution of 2,4-dichloro-3-nitroquinoline (7.22 g, 26.7 mmol) in dichloromethane (100 mL). A solution of 4-(aminomethyl)tetrahydro-2H-thiopyran-4-ol (4.12 g, 28.0 mmol) in dichloromethane (30 mL) was added dropwise. The reaction mixture was stirred at ambient temperature overnight and then concentrated under reduced pressure. The orange residue was combined with saturated aqueous sodium bicarbonate (50 mL) and ethyl acetate (40 mL), sonicated for 10 minutes, and then filtered. The isolated solid was washed extensively with water and then dried to provide 5.63 g of 4-{[(2-chloro-3-nitroquinolin-4-yl)amino]methyl}tetrahydro-2H-thiopyran-4-ol as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07884207B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-ab8231b307eb4352a590b44de811bb5e
출처 메모uspto-grants-2011_02