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

HRID 1780667
ノート
印刷プレビュー

反応式

HRID 1780667 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-db9a4bd0f09d4b189a7e8cc0650286e6
出典データセット
uspto-grants-1997_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05631257

反応ノート

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