돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 889423생성일: 2026년 10월 27일

1H-1,2,4-Triazole → N,N-dimethyl-2-(3-nitro-5-(1H-1,2,4-triazol-1-yl)phenoxy)ethanamine

https://huagongshe.com/reaction/889423

반응식

참여 물질

역할이름HCID투입량
반응물1H-1,2,4-TriazoleHCID 9257—
반응물Potassium CarbonateHCID 11430—
반응물2-(3-bromo-5-nitrophenoxy)-N,N-dimethylethanamineHCID 59313993—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매DichloromethaneHCID 6344—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물N,N-dimethyl-2-(3-nitro-5-(1H-1,2,4-triazol-1-yl)phenoxy)ethanamineHCID 5931385157%

반응 단계

Intermediate 16A (200 mg, 0.69 mmol), copper(I) iodide (65.9 mg, 0.35 mmol), potassium carbonate (287 mg, 2.1 mmol) and 1H-1,2,4-triazole (143 mg, 2.075 mmol) in NMP (2 mL) were heated at 120° C. for 6 hours. The reaction mixture was diluted with dichloromethane, and filtered through a plug of silica gel and washed with ethyl acetate. The filtrate was concentrated, and the residue was purified by reverse phase HPLC to obtain Intermediate 16B (109 mg, 56.8% yield) as a yellow solid. HPLC: Rt=0.74 min. (PHENOMENEX® Luna 5 micron C18 4.6×30 mm, 10-90% aqueous methanol containing 0.1% TFA, 2 min. gradient, flow rate=5 mL/min, detection at 254 nm). MS (ES): m/z=278.08 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08252795B2
출처 데이터셋uspto-grants-2012_08
ORD IDord-9cd1b105d2e44f558f20b82ae5ba426f
출처 메모uspto-grants-2012_08