Ethanol → 3-[1-(Benzo[b]thiophen-2-yl)cyclobutyl]-5,6-dihydroimidazo[2,1-b]thiazole hydrobromide

HRID 635372노트

반응식

HRID 635372 반응식
[S:1]1[C:5]([C:6]2([C:10](=O)[CH2:11][Br:12])[CH2:9][CH2:8][CH2:7]2)=[CH:4][C:3]2[CH:14]=[CH:15][CH:16]=[CH:17][C:2]1=2.[NH:18]1[CH2:22][CH2:21][NH:20][C:19]1=[S:23].C(O)C>C(O)(=O)C>[BrH:12].[S:1]1[C:5]([C:6]2([C:10]3[N:20]4[CH2:21][CH2:22][N:18]=[C:19]4[S:23][CH:11]=3)[CH2:9][CH2:8][CH2:7]2)=[CH:4][C:3]2[CH:14]=[CH:15][CH:16]=[CH:17][C:2]1=2

참가 물질

5

반응물 3

HCID 702EthanolHCID 2723650EthylenethioureaHCID 212585221-[1-(Benzo[b]thiophen-2-yl)cyclobutyl]-2-bromoethanone

생성물 1

HCID 212584013-[1-(Benzo[b]thiophen-2-yl)cyclobutyl]-5,6-dihydroimidazo[2,1-b]thiazole hydrobromide수율 52.4%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

A mixture of 1-[1-(benzo[b]thiophen-2-yl)cyclobutyl]-2-bromoethanone (0.42 g), imidazolidine-2-thione (0.14 g), ethanol (15 ml) and acetic acid (10 ml) was heated under reflux for 18 hours then allowed to cool to ambient temperature. The solvents were removed in vacuo and the residue was triturated with ether (30 ml). The resulting solid was collected by filtration, dried in vacuo at 40° C. and crystallised from ethanol. The resulting product was collected by filtration, washed with ethanol (3 ml) and dried in vacuo at 40° C. to give 3-[1-(benzo[b]thiophen-2-yl)cyclobutyl]-5,6-dihydroimidazo[2,1-b]thiazole hydrobromide as an off-white solid (0.28 g), m.p. 240-242° C.

후처리

  1. temperaturewas heated
  2. temperatureunder reflux for 18 hours
  3. customThe solvents were removed in vacuo
  4. customthe residue was triturated with ether (30 ml)
  5. filtrationThe resulting solid was collected by filtration
  6. customdried in vacuo at 40° C.
  7. customcrystallised from ethanol
  8. filtrationThe resulting product was collected by filtration
  9. washwashed with ethanol (3 ml)
  10. customdried in vacuo at 40° C.

출처 및 근거

ORD 기록
ord-eec96c602eda4102991dd53be5d6e396
출처 데이터셋
uspto-grants-2001_02
특허 번호
US06187802B1

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