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1-(2-Pyridyl)piperazine → 6-Methoxy-3-[1-(2-pyridyl)piperazinyl]-1,2-benzisoxazole

HRID 2396733
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인쇄 미리보기

반응식

HRID 2396733 반응식
Cl[C:2]1[C:6]2[CH:7]=[CH:8][C:9]([O:11][CH3:12])=[CH:10][C:5]=2[O:4][N:3]=1.[N:13]1[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=1[N:19]1[CH2:24][CH2:23][NH:22][CH2:21][CH2:20]1>CO>[CH3:12][O:11][C:9]1[CH:8]=[CH:7][C:6]2[C:2]([CH:20]3[CH2:21][NH:22][CH2:23][CH2:24][N:19]3[C:14]3[CH:15]=[CH:16][CH:17]=[CH:18][N:13]=3)=[N:3][O:4][C:5]=2[CH:10]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 944591-(2-Pyridyl)piperazineHCID 158169243-Chloro-6-methoxy-1,2-benzoxazole

생성물 1

HCID 537029076-Methoxy-3-[1-(2-pyridyl)piperazinyl]-1,2-benzisoxazole수율 34.5%

시약·촉매·용매 1

HCID 887Methanol용매

반응 조건

온도
140 °C

실험 절차

A sealed tube was charged with 3-chloro-6-methoxy-1,2-benzisoxazole (0.25 g, 1.4mmol) and 1-(2-pyridyl)piperazine (0.67 g, 4 mmol) and heated to 140° C. overnight. The reaction was cooled to room temperature, diluted with methanol, and concentrated in vacuo. The material was flash chromatographed (silica gel) eluting with CH2Cl2. The material was further purified through recrystallization from 1,2-dichloroethane/pet. ether to afford 0.15 g of the product, m.p.=123°-124° C.

후처리

  1. temperatureThe reaction was cooled to room temperature
  2. concentrationconcentrated in vacuo
  3. customchromatographed (silica gel)
  4. washeluting with CH2Cl2
  5. customThe material was further purified through recrystallization from 1,2-dichloroethane/pet. ether

출처 및 근거

ORD 기록
ord-af5a1197ccb344068d4da4f081ed5315
출처 데이터셋
uspto-grants-1996_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05494908

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