Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
1H-1,2,4-Triazole → N,N-dimethyl-2-(3-nitro-5-(1H-1,2,4-triazol-1-yl)phenoxy)ethanamine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 1H-1,2,4-Triazole | HCID 9257 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 2-(3-bromo-5-nitrophenoxy)-N,N-dimethylethanamine | HCID 59313993 | — |
| 촉매 | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 생성물 | N,N-dimethyl-2-(3-nitro-5-(1H-1,2,4-triazol-1-yl)phenoxy)ethanamine | HCID 59313851 | 57% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08252795B2 |
| 출처 데이터셋 | uspto-grants-2012_08 |
| ORD ID | ord-9cd1b105d2e44f558f20b82ae5ba426f |
| 출처 메모 | uspto-grants-2012_08 |