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1,3-Dibromopropane → 5-(3-bromopropyl)oxy-4-propyl-N-(4-chlorophenyl)indole

HRID 342770
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HRID 342770 반응식
[OH:1][C:2]1[C:3]([CH2:18][CH2:19][CH3:20])=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([C:11]1[CH:16]=[CH:15][C:14]([Cl:17])=[CH:13][CH:12]=1)[CH:6]=[CH:5]2.C(=O)([O-])[O-].[K+].[K+].[Br:27][CH2:28][CH2:29][CH2:30]Br>CN(C)C=O.C(OCC)(=O)C.[Cl-].[NH4+]>[Br:27][CH2:28][CH2:29][CH2:30][O:1][C:2]1[C:3]([CH2:18][CH2:19][CH3:20])=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([C:11]1[CH:16]=[CH:15][C:14]([Cl:17])=[CH:13][CH:12]=1)[CH:6]=[CH:5]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 80011,3-DibromopropaneHCID 11430Potassium CarbonateHCID 537470165-hydroxy-4-propyl-N-(4-chlorophenyl)indole

생성물 1

HCID 544467205-(3-bromopropyl)oxy-4-propyl-N-(4-chlorophenyl)indole

시약·촉매·용매 3

HCID 6228Dimethylformamide용매HCID 8857Ethyl Acetate
용매
HCID 25517Ammonium Chloride용매

실험 절차

To a solution of 5-hydroxy-4-propyl-N-(4-chlorophenyl)indole (Step D; 500 mg, 1.75 mmol) and potassium carbonate (484 mg, 3.50 mmol) in 7 mL of dimethylformamide (DMF) was added 1,3-dibromopropane (1.77 g, 8.75 mmol). The mixture was stirred at ambient temperature for 2 hours and diluted with ethyl acetate and saturated aqueous ammonium chloride. The aqueous phase was extracted with ethyl acetate and the combined organic extracts were washed brine, dried over magnesium sulfate, filtered, concentrated in vacuo, and the crude residue was used as is in the next step.

후처리

  1. extractionThe aqueous phase was extracted with ethyl acetate
  2. washthe combined organic extracts were washed brine
  3. dry with materialdried over magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-9a8828c43a1749eca064fb2fec71abed
출처 데이터셋
uspto-grants-1999_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05859051

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