Methanol → 2-Amino-4-(4-fluorophenyl)-5-[2-[4-(6-fluorobenzofuran-3-yl)piperidin-1-yl]ethyl]thiazole

HRID 393176노트

반응식

HRID 393176 반응식
Br.[NH2:2][C:3]1[S:4][C:5]([CH2:15][CH2:16]Br)=[C:6]([C:8]2[CH:13]=[CH:12][C:11]([F:14])=[CH:10][CH:9]=2)[N:7]=1.Cl.[F:19][C:20]1[CH:34]=[CH:33][C:23]2[C:24]([CH:27]3[CH2:32][CH2:31][NH:30][CH2:29][CH2:28]3)=[CH:25][O:26][C:22]=2[CH:21]=1.C(N(C(C)C)CC)(C)C.CO>O>[NH2:2][C:3]1[S:4][C:5]([CH2:15][CH2:16][N:30]2[CH2:31][CH2:32][CH:27]([C:24]3[C:23]4[CH:33]=[CH:34][C:20]([F:19])=[CH:21][C:22]=4[O:26][CH:25]=3)[CH2:28][CH2:29]2)=[C:6]([C:8]2[CH:13]=[CH:12][C:11]([F:14])=[CH:10][CH:9]=2)[N:7]=1

참가 물질

6

실험 절차

A mixture of 0.917 g of 2-amino-5-(2-bromoethyl)-4-(4-fluorophenyl)thiazole hydrobromide, 0.511 g of 4-(6-fluorobenzofuran-3-yl)piperidine hydrochloride, 1.5 ml of diisopropylethylamine and 3 ml of methanol was stirred with heating under reflux for 12 hours. The reaction mixture was cooled to room temperature and then poured into water, followed by extraction with chloroform. The extract solution was dried over magnesium sulfate, and then the solvent was distilled off under reduced pressure, after which ether was added to the residue and the crystals were collected by filtration. The crystals were recrystallized from ethanol to obtain 0.57 g of 2-amino-4-(4-fluorophenyl)-5-[2-[4-(6-fluorobenzofuran-3-yl)piperidin-1-yl]ethyl]thiazole.

후처리

  1. temperaturewith heating
  2. temperatureunder reflux for 12 hours
  3. extractionfollowed by extraction with chloroform
  4. dry with materialThe extract solution was dried over magnesium sulfate
  5. distillationthe solvent was distilled off under reduced pressure
  6. additionafter which ether was added to the residue
  7. filtrationthe crystals were collected by filtration
  8. customThe crystals were recrystallized from ethanol

출처 및 근거

ORD 기록
ord-093a27cf382844b68d0c2b55813f5c29
출처 데이터셋
uspto-grants-2004_10
특허 번호
US06806275B2

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