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Sodium Hydroxide → 2-[2-(4-benzyl-1-piperazinyl)ethyl]-1-methyl-1H-naphth[1,2-d]imidazole

HRID 2198993
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HRID 2198993 반응식
Br[C:2]1[C:30]2[C:25](=[CH:26][CH:27]=[CH:28][CH:29]=2)[C:5]2[N:6]([CH3:24])[C:7]([CH2:9][CH2:10][N:11]3[CH2:16][CH2:15][N:14]([CH2:17][C:18]4[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=4)[CH2:13][CH2:12]3)=[N:8][C:4]=2[CH:3]=1.[OH-].[Na+]>C1(C)C=CC=CC=1>[CH2:17]([N:14]1[CH2:15][CH2:16][N:11]([CH2:10][CH2:9][C:7]2[N:6]([CH3:24])[C:5]3[C:25]4[C:30]([CH:2]=[CH:3][C:4]=3[N:8]=2)=[CH:29][CH:28]=[CH:27][CH:26]=4)[CH2:12][CH2:13]1)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 140725035-Bromo-2-[2-(4-benzyl-1-piperazinyl)ethyl]-1-methyl-1H-naphth[1,2-d]imidazole

생성물 1

HCID 140725102-[2-(4-benzyl-1-piperazinyl)ethyl]-1-methyl-1H-naphth[1,2-d]imidazole수율 58.4%

시약·촉매·용매 1

HCID 1140Toluene용매2회

실험 절차

3.9 cc of toluene containing 2.62 g (0.013 mole) of (CH3OCH2CH2O)2NaAlH2 is added to a solution of 4.13 g (0.0089 mole) of the compound of Example 16 in 80 cc of toluene and the obtained mixture is refluxed with stirring under argon atmosphere. After 6 hours, when the reaction, which is followed by thin layer chromatography, is completed, 100 cc of 5% NaOH is added to the mixture and the toluene phase is separated and washed with a saturated NaCl solution. Upon evaporating the solvent, a crude product is obtained which is recrystallized from ethyl acetate:hexane 1:1, yielding 2 g of the compound of the title. M.p. 144°-46° C.

후처리

  1. temperaturethe obtained mixture is refluxed
  2. customwhen the reaction, which
  3. customthe toluene phase is separated
  4. washwashed with a saturated NaCl solution
  5. customUpon evaporating the solvent
  6. customa crude product is obtained which
  7. customis recrystallized from ethyl acetate:hexane 1:1

출처 및 근거

ORD 기록
ord-f8cb66d3303c423b8ce410b382419f62
출처 데이터셋
uspto-grants-1982_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04360674

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