N-Methylbenzylamine → 3-Methyl-6-[2-(N-methyl-N-benzylamino)ethyl]benzothiazolinone

HRID 1614218노트

반응식

HRID 1614218 반응식
[CH3:1][NH:2][CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[CH3:10][N:11]1[C:15]2[CH:16]=[CH:17][C:18]([CH2:20][CH2:21]Br)=[CH:19][C:14]=2[S:13](=[O:23])[CH2:12]1>O1CCOCC1>[CH3:10][N:11]1[C:15]2[CH:16]=[CH:17][C:18]([CH2:20][CH2:21][N:2]([CH3:1])[CH2:3][C:4]3[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=3)=[CH:19][C:14]=2[S:13](=[O:23])[CH2:12]1

참가 물질

4

반응물 2

HCID 7669N-MethylbenzylamineHCID 701838363-Methyl-6-(2-bromoethyl)benzothiazolinone

생성물 1

HCID 678520773-Methyl-6-[2-(N-methyl-N-benzylamino)ethyl]benzothiazolinone

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

0.04 mol of N-methyl-N-benzylamine and 0.02 mol of 3-methyl-6-(2-bromoethyl)benzothiazolinone, the latter being dissolved beforehand in 120 cm3 of dioxane, are introduced into a 100-cm3 ground-necked flask fitted with a reflux condenser. The mixture is heated to reflux for 96 hours with magnetic stirring. After cooling, the reaction mixture is filtered and the filtrate is then evaporated on a water bath under vacuum. The residue is taken up with 50 cm3 and alkalinized with 10 cm3 of normal sodium hydroxide solution.

후처리

  1. additionare introduced into a 100-cm3 ground-necked flask
  2. customfitted with a reflux condenser
  3. temperatureThe mixture is heated
  4. temperatureto reflux for 96 hours with magnetic stirring
  5. temperatureAfter cooling
  6. filtrationthe reaction mixture is filtered
  7. customthe filtrate is then evaporated on a water bath under vacuum

출처 및 근거

ORD 기록
ord-e3a39a2074214afea6b5a631a4ac8c34
출처 데이터셋
uspto-grants-1993_03
특허 번호
US05196434

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