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Methyl iodide → 1,1-Dimethyl-4-(benzoxazol-2-yl)homopiperazinium iodide

HRID 1780667
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인쇄 미리보기

반응식

HRID 1780667 반응식
[CH3:1][N:2]1[CH2:8][CH2:7][CH2:6][N:5]([C:9]2[O:10][C:11]3[CH:17]=[CH:16][CH:15]=[CH:14][C:12]=3[N:13]=2)[CH2:4][CH2:3]1.[CH3:18][I:19]>O1CCCC1>[I-:19].[CH3:1][N+:2]1([CH3:18])[CH2:8][CH2:7][CH2:6][N:5]([C:9]2[O:10][C:11]3[CH:17]=[CH:16][CH:15]=[CH:14][C:12]=3[N:13]=2)[CH2:4][CH2:3]1
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참가 물질

4

반응물 2

HCID 6328Methyl iodideHCID 105856212-(4-Methyl-1-homopiperazinyl)benzoxazole

생성물 1

HCID 190472911,1-Dimethyl-4-(benzoxazol-2-yl)homopiperazinium iodide

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A 200 mg portion of 2-(4-methyl-1-homopiperazinyl)-benzoxazole was dissolved in 5 ml of tetrahydrofuran (THF). Under cooling with ice, 0.064 ml of methyl iodide was added to the thus prepared solution, and the reaction was carried out for 1 hour at the same temperature and then for 2 hours at room temperature. The reaction solution was concentrated under a reduced pressure, and 5 ml of acetone was added to the resulting residue. The precipitate thus formed was collected by filtration, washed with acetone and then dried to obtain 320 mg of the title compound.

후처리

  1. additionwas added to the thus prepared solution
  2. waitfor 2 hours at room temperature
  3. concentrationThe reaction solution was concentrated under a reduced pressure, and 5 ml of acetone
  4. additionwas added to the resulting residue
  5. customThe precipitate thus formed
  6. filtrationwas collected by filtration
  7. washwashed with acetone
  8. customdried

출처 및 근거

ORD 기록
ord-db9a4bd0f09d4b189a7e8cc0650286e6
출처 데이터셋
uspto-grants-1997_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05631257

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