Sodium hydride → 4-(6-Ethoxytetralin-2-yloxy)quinazoline

HRID 1385891노트

반응식

HRID 1385891 반응식
[CH2:1]([O:3][C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][CH:13]=1)[CH2:10][CH:9]([OH:14])[CH2:8][CH2:7]2)[CH3:2].[H-].[Na+].Cl[C:18]1[C:27]2[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=2)[N:21]=[CH:20][N:19]=1>C1COCC1.CCOCC>[CH2:1]([O:3][C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][CH:13]=1)[CH2:10][CH:9]([O:14][C:18]1[C:27]3[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=3)[N:21]=[CH:20][N:19]=1)[CH2:8][CH2:7]2)[CH3:2]

참가 물질

6

반응물 3

HCID 24758Sodium hydrideHCID 788644-ChloroquinazolineHCID 118302726-Ethoxytetralin-2-ol

생성물 1

HCID 110126414-(6-Ethoxytetralin-2-yloxy)quinazoline

시약·촉매·용매 2

HCID 3283Diethyl Ether용매HCID 8028Tetrahydrofuran용매

실험 절차

2.57 g (13.3 mmol) of 6-ethoxytetralin-2-ol in 5 ml of THF were added, with ice-cooling, to a suspension of 400 mg of NaH (80% pure, 13.3 mmol in 40 ml of THF). The mixture was subsequently refluxed for 1 hour and cooled to room temperature, and 2.0 g (12.2 mmol) of 4-chloroquinazoline were added. The mixture was refluxed for 24 hours and cooled and then diluted with ether and washed with saturated sodium hydrogen carbonate and saturated sodium chloride solution. After the organic phase had been dried and concentrated, the residue was chromatographed on silica gel using petroleum ether/ethyl acetate (9:1, 8:2). This gave 2.39 g (61% of theory) of colorless crystals (m.p.115-117° C.).

후처리

  1. temperatureThe mixture was subsequently refluxed for 1 hour
  2. temperatureThe mixture was refluxed for 24 hours
  3. temperaturecooled
  4. washwashed with saturated sodium hydrogen carbonate and saturated sodium chloride solution
  5. customAfter the organic phase had been dried
  6. concentrationconcentrated
  7. customthe residue was chromatographed on silica gel

출처 및 근거

ORD 기록
ord-7b9e9785ddf64b9686c66a0c08697aac
출처 데이터셋
uspto-grants-2001_07
특허 번호
US06265398B1

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