HCID 4431756, 화합물 → 4,5,6,7-Tetrahydro-N6-propyl-2,6-benzothiazolediamine

HRID 1897736

반응식

HRID 1897736 반응식
[CH2:1](S([O-])(=O)=O)[CH2:2][CH3:3].[NH2:8][C:9]1[S:10][C:11]2[CH2:17][CH:16]([NH2:18])[CH2:15][CH2:14][C:12]=2[N:13]=1>>[NH2:8][C:9]1[S:10][C:11]2[CH2:17][CH:16]([NH:18][CH2:1][CH2:2][CH3:3])[CH2:15][CH2:14][C:12]=2[N:13]=1

참가 물질

3

실험 절차

In some embodiments, step one of the process may include the additional steps of heating a diamine to form a solution or melt in a heating step and adding the n-propyl halide or n-propyl sulfonate slowly over a period of time from, for example, about 0.5 hours to about 5 hours, in an additional step. In other embodiments, after the n-propyl halide or n-propyl sulfonate has been completely added to the 2,6 diamino-4,5,6,7-tetrahydro-benzothiazole, the reaction may continue under heating for an additional period of time ranging from, for example, about 1 hour to about 12 hours, in a reaction step. In certain embodiments, the reaction mixture may be mixed by, for example, stirring for one or more of the steps above or the reaction mixture may be continually stirred from the heating step to the reaction step. Following the reaction step, the reaction mixture may be cooled and the 2-amino-4,5,6,7-tetrahydro-6-(propylamino)benzothiazole may be isolated and purified.

후처리

  1. customto form a solution
  2. customthe reaction
  3. temperatureunder heating for an additional period of time
  4. customfor example, about 1 hour to about 12 hours
  5. customin a reaction step
  6. additionIn certain embodiments, the reaction mixture may be mixed by, for example
  7. stirringmay be continually stirred from the heating step to the reaction step
  8. customthe reaction step
  9. temperaturethe reaction mixture may be cooled

출처 및 근거

ORD 기록
ord-4fd1efac75b34fc896eac6da9a96a062
출처 데이터셋
uspto-grants-2013_08
특허 번호
US08519148B2

연결된 노트

불러오는 중…