Hydrochloric Acid → Tiagabine

HRID 619242노트

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HRID 619242 반응식
CC[O:3][C:4]([C@H:6]1[CH2:11][N:10]([CH2:12][CH2:13][CH:14]=[C:15]([C:22]2[S:26][CH:25]=[CH:24][C:23]=2[CH3:27])[C:16]2[S:20][CH:19]=[CH:18][C:17]=2[CH3:21])[CH2:9][CH2:8][CH2:7]1)=[O:5].Cl>O>[CH3:27][C:23]1[CH:24]=[CH:25][S:26][C:22]=1[C:15]([C:16]1[S:20][CH:19]=[CH:18][C:17]=1[CH3:21])=[CH:14][CH2:13][CH2:12][N:10]1[CH2:11][C@H:6]([C:4]([OH:5])=[O:3])[CH2:7][CH2:8][CH2:9]1

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 11555813PIP017

생성물 1

HCID 60648Tiagabine수율 90.3%

시약·촉매·용매 1

HCID 962Water용매

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온도
88 °C

실험 절차

To a 1 L flask, 50 g of tiagabine ethyl ester, 575 ml of water and 25 g of conc. hydrochloric acid were charged. The mixture was heated to reflux for 1 hour and then ethanol/water, a total of 200 ml, was distilled off over a period of 4 hours. The reaction solution was cooled to 88° C. and then an additional 23.5 g of conc. hydrochloric acid was added. The solution was gradually cooled to room temperature (22° C.) while the reaction was stirred for 18 hours. The resulting precipitate was collected by filtration and was washed with 20 ml of water. The product was dried under vacuum at room temperature to give 42.0 g of Tiagabine, hydrochloride.

후처리

  1. temperatureThe mixture was heated
  2. temperatureto reflux for 1 hour
  3. distillationethanol/water, a total of 200 ml, was distilled off over a period of 4 hours
  4. additionan additional 23.5 g of conc. hydrochloric acid was added
  5. temperatureThe solution was gradually cooled to room temperature (22° C.) while the reaction
  6. filtrationThe resulting precipitate was collected by filtration
  7. washwas washed with 20 ml of water
  8. customThe product was dried under vacuum at room temperature

출처 및 근거

ORD 기록
ord-ac47111540ec4257b45a58f85740db35
출처 데이터셋
uspto-grants-1999_09
특허 번호
US05958951

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