Imidazole → HCID 20564366, 화합물

HRID 848752노트

반응식

HRID 848752 반응식
[NH:1]1[CH:5]=[CH:4][N:3]=[CH:2]1.[H-].[Na+].[CH:8]([N:11]([CH:23]([CH3:25])[CH3:24])[C:12](=[O:22])[CH:13](Cl)[C:14]1[CH:19]=[CH:18][C:17]([Cl:20])=[CH:16][CH:15]=1)([CH3:10])[CH3:9]>CN(C)C=O>[CH:23]([N:11]([CH:8]([CH3:10])[CH3:9])[C:12](=[O:22])[CH:13]([C:14]1[CH:15]=[CH:16][C:17]([Cl:20])=[CH:18][CH:19]=1)[N:1]1[CH:5]=[CH:4][N:3]=[CH:2]1)([CH3:24])[CH3:25]

참가 물질

5

실험 절차

While stirring, a solution of 4.5 g of imidazole in 30 ml of dimethylformamide is dripped into a suspension of 1.3 g of sodium hydride in 30 ml of dimethylformamide. When no more gas evolves, a solution of 13.6 g of α-chloro-α-(4-chlorophenyl)-acetic acid-diisopropyl amide (see d)) in 100 ml of dimethylformamide is dripped in and the mixture is stirred overnight at room temperature. The oil which remains after the solvent has been evaporated off is taken up in 100 ml of dichloromethane and shaken 5 times, each time with 100 ml of 5% strength sodium chloride solution. The organic phase is then concentrated and chromatographed on silica gel (25×6 cm) using dichloromethane/acetone (9:1). After 2 l of first runnings have been separated off, the product fractions are obtained from which, after concentration and trituration with 10 ml of diisopropyl ether, 8.9 g of colorless crystals (m.p.: 112° C.) are isolated.

후처리

  1. stirringis stirred overnight at room temperature
  2. customhas been evaporated off
  3. stirringshaken 5 times
  4. concentrationThe organic phase is then concentrated
  5. customchromatographed on silica gel (25×6 cm)
  6. customAfter 2 l of first runnings have been separated off
  7. customthe product fractions are obtained from which
  8. concentrationafter concentration and trituration with 10 ml of diisopropyl ether, 8.9 g of colorless crystals (m.p.: 112° C.)
  9. customare isolated

출처 및 근거

ORD 기록
ord-08e6e8fed4a840a288729760acdb99f1
출처 데이터셋
uspto-grants-1981_10
특허 번호
US04297364

반응 노트

불러오는 중…