Hydrochloric Acid → Ticlopidine Hydrochloride

HRID 46678

반응식

HRID 46678 반응식
C=O.[CH3:3]S(O)(=O)=O.[Cl:8][C:9]1[CH:23]=[CH:22][CH:21]=[CH:20][C:10]=1[CH2:11][NH:12][CH2:13][CH2:14][C:15]1[S:16][CH:17]=[CH:18][CH:19]=1.[OH-].[Na+].Cl>CN(C)C=O.C(O)C>[ClH:8].[Cl:8][C:9]1[CH:23]=[CH:22][CH:21]=[CH:20][C:10]=1[CH2:11][N:12]1[CH2:13][CH2:14][C:15]2[S:16][CH:17]=[CH:18][C:19]=2[CH2:3]1

참가 물질

8

반응 조건

온도
20 °C

실험 절차

To 2.25 g (0.075 M) paraformaldehyde suspended in 20 ml dimethylformamide are added 9.61 g (0.1 M) methanesulfonic acid. The medium being at a temperature of 72° C., 13 g (0.05 M) N-(2-chloro-benzyl)-2-(2-thienyl)ethylamine dissolved in 5 ml dimethylformamide are added over 2 minutes. The temperature of the reaction medium reaches 90° C. The reaction medium is then cooled to 20° C. and poured over 50 ml 4N sodium hydroxide. The material is extracted with 1×30 ml and then 1×20 ml methylene chloride. The organic phases are combined, dried over sodium sulfate and evaporated, to give an oil which is taken up into 30 ml ethanol in which are dissolved 0.15 mole gaseous hydrochloric acid. After partial evaporation of the ethanol, the desired product precipitates out. It is filtered, washed with acetone and dried, to give 11.35 g 5-(2-chloro-benzyl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridine hydrochloride (Yield: 75.6%).

후처리

  1. additionare added over 2 minutes
  2. custommedium reaches 90° C
  3. extractionThe material is extracted with 1×30 ml
  4. dry with materialdried over sodium sulfate
  5. customevaporated
  6. customto give an oil which
  7. customAfter partial evaporation of the ethanol
  8. customthe desired product precipitates out
  9. filtrationIt is filtered
  10. washwashed with acetone
  11. customdried

출처 및 근거

ORD 기록
ord-6a087057b35f4230abd8f03b91abb4e0
출처 데이터셋
uspto-grants-1979_11
특허 번호
US04174448

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