Cerium(III) chloride → 3-(2-(4-((1H-Benzo[D]imidazol-2-YL)(hydroxy)methyl)phenoxy)pyridin-3-YL)cyclopent-2-enol

HRID 1880162

반응식

HRID 1880162 반응식
[NH:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[C:10]([C:12]1[CH:30]=[CH:29][C:15]([O:16][C:17]2[C:22]([C:23]3[CH2:27][CH2:26][C:25](=[O:28])[CH:24]=3)=[CH:21][CH:20]=[CH:19][N:18]=2)=[CH:14][CH:13]=1)=[O:11].[Cl-].[Ce+3].[Cl-].[Cl-].[B-].[Na+]>O1CCCC1.CO>[NH:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[CH:10]([OH:11])[C:12]1[CH:30]=[CH:29][C:15]([O:16][C:17]2[C:22]([C:23]3[CH2:27][CH2:26][CH:25]([OH:28])[CH:24]=3)=[CH:21][CH:20]=[CH:19][N:18]=2)=[CH:14][CH:13]=1

참가 물질

6

반응 조건

온도
0 °C

실험 절차

A suspension of 3-(2-(4-(1H-benzo[d]imidazole-2-carbonyl)phenoxy)pyridin-3-yl)cyclopent-2-enone (2125 mg, 5.37 mmol) and cerium (iii) chloride (1325 mg, 5.37 mmol) in tetrahydrofuran (300 mL) and methanol (30.0 mL) was cooled to 0° C. under nitrogen. Sodium borohydrate (813 mg, 21.50 mmol) was added in 4 lots over 20 min. The reaction was warmed to 23° C. over 2 h. After a total reaction time of 4 h, the reaction was quenched with saturated ammonium chloride solution (10 ml, slowly—effervescence). The solution was diluted with EtOAc (500 mL) and washed with saturated ammonium chloride solution (100 mL) and brine (100 mL), dried over MgSO4, concentrated in vacuo and purified by silica gel chromatography (eluant: 1-8% methanol/dichloromethane), affording the product as a yellow film.

후처리

  1. temperatureThe reaction was warmed to 23° C. over 2 h
  2. customAfter a total reaction time of 4 h, the reaction was quenched with saturated ammonium chloride solution (10 ml
  3. additionThe solution was diluted with EtOAc (500 mL)
  4. washwashed with saturated ammonium chloride solution (100 mL) and brine (100 mL)
  5. dry with materialdried over MgSO4
  6. concentrationconcentrated in vacuo
  7. custompurified by silica gel chromatography (eluant: 1-8% methanol/dichloromethane)
  8. customaffording the product as a yellow film

출처 및 근거

ORD 기록
ord-6e6401a168784fb885653924ffc7afdb
출처 데이터셋
uspto-grants-2012_11
특허 번호
US08318718B2

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