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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 44771생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/44771

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 번호US08541438B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-a77b4c6687a8443dabe3aa1084d8b2a3
출처 메모uspto-grants-2013_09