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Water → Methyl 3-methyl-1-{3-(phenyl)propyl}-1H-indole-6-carboxylate

HRID 380431
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HRID 380431 반응식
[CH3:1][C:2]1[C:10]2[C:5](=[CH:6][C:7]([C:11]([O:13][CH3:14])=[O:12])=[CH:8][CH:9]=2)[NH:4][CH:3]=1.Br[CH2:16][CH2:17][CH2:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1.[OH-].[Na+].O>CC(C)=O>[CH3:1][C:2]1[C:10]2[C:5](=[CH:6][C:7]([C:11]([O:13][CH3:14])=[O:12])=[CH:8][CH:9]=2)[N:4]([CH2:16][CH2:17][CH2:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 12503(3-Bromopropyl)benzeneHCID 14798Sodium HydroxideHCID 21938240Methyl 3-methyl-1H-indole-6-carboxylate

생성물 1

HCID 22663283Methyl 3-methyl-1-{3-(phenyl)propyl}-1H-indole-6-carboxylate수율 71.4%

시약·촉매·용매 1

HCID 180Acetone
용매

실험 절차

A stirred solution of methyl 3-methyl-1 H-indole-6-carboxylate (0.5 g, Reference Example 30) in acetone (35 ml) was treated with 1-bromo-3-phenylpropane (0.577 g) and sodium hydroxide (0.116 g). The mixture was stirred at room temperature for 12 hours then poured into water (35 ml) and then extracted three times with ethyl acetate (50 ml). The combined extracts were washed with dilute hydrochloric acid (50 ml, 1N) then with saturated sodium bicarbonate solution (50 ml), then dried over magnesium sulphate and then evaporated. The residue was subjected to flash column chromatography on silica eluting with a mixture of ethyl acetate and hexane (50:1, v/v) to yield the title compound (0.58 g).

후처리

  1. extractionextracted three times with ethyl acetate (50 ml)
  2. washThe combined extracts were washed with dilute hydrochloric acid (50 ml, 1N)
  3. dry with materialwith saturated sodium bicarbonate solution (50 ml), then dried over magnesium sulphate
  4. customevaporated
  5. additionThe residue was subjected to flash column chromatography on silica eluting with a mixture of ethyl acetate and hexane (50:1

출처 및 근거

ORD 기록
ord-86d7fc3bad1c4c8895d7c05327ba3f80
출처 데이터셋
uspto-grants-2001_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06303600B1

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