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

HRID 2186793노트

반응식

HRID 2186793 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-a2d88f472a1a4cef9afdb1e506be7352
출처 데이터셋
uspto-grants-2002_06
특허 번호
US06407121B1

반응 노트

불러오는 중…