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Triethylamine → n-[2-[2-(1,1-Dimethyl-2-propenyl)-1h-indol-3-yl]ethyl]-carbamic acid phenylmethyl ester

HRID 1071079
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HRID 1071079 반응식
[CH3:1][C:2]([C:6]1[NH:7][C:8]2[C:13]([C:14]=1[CH2:15][CH2:16][NH2:17])=[CH:12][CH:11]=[CH:10][CH:9]=2)([CH3:5])[CH:3]=[CH2:4].CCN(CC)CC.[CH2:25]([O:32][C:33](Cl)=[O:34])[C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1>C(Cl)Cl>[C:26]1([CH2:25][O:32][C:33](=[O:34])[NH:17][CH2:16][CH2:15][C:14]2[C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[NH:7][C:6]=2[C:2]([CH3:1])([CH3:5])[CH:3]=[CH2:4])[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1
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참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 10387Benzyl chloroformateHCID 223967402-(1,1-dimethyl-2-propenyl)-1H-indole-3-ethanamine

생성물 1

HCID 69792966n-[2-[2-(1,1-Dimethyl-2-propenyl)-1h-indol-3-yl]ethyl]-carbamic acid phenylmethyl ester

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

To a solution of 2-(1,1-dimethyl-2-propenyl)-1H-indole-3-ethanamine (0.707 g, 3.07 mmol) in dry CH2Cl2 (30 mL) at 0° C. under argon was added NEt3 (0.98 mL, 6.93 mmol) and BnOC(O)Cl (1.10 mL, 7.32 mmol). The reaction was permitted to warm to rt while stirring overnight. It was diluted with CH2Cl2, and extracted with cold H2O. The CH2Cl2 layer was separated. The H2O layer was re-extracted with CH2Cl2. The combined CH2Cl2 extracts were washed with satd aq NaHCO3 and brine, dried, filtered and concentrated to give an oil. This oil was purified by silica chromatography to provide the title compound: TLC Rf=0.34 (CH2Cl2); MS (EI) m/z 362.3, 254, 211, 198, 182. 168, 167, 108, 91, 77, 65, 51; 1H NMR (300 MHz, CDCl3) δ 7.89 (1H), 7.56 (1H), 7.33-7.26 (6H), 7.10 (2H), 6.12 (1H), 5.18-5.12 (2H), 5.12 (2H), 4.87 (1H), 3.47 (2H), 3.07 (2H), 1.53 (6H).

후처리

  1. extractionextracted with cold H2O
  2. customThe CH2Cl2 layer was separated
  3. extractionThe H2O layer was re-extracted with CH2Cl2
  4. washThe combined CH2Cl2 extracts were washed with satd aq NaHCO3 and brine
  5. customdried
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customto give an oil
  9. customThis oil was purified by silica chromatography

출처 및 근거

ORD 기록
ord-89b9861dd3bb48d0a1aa5e20879ba63f
출처 데이터셋
uspto-grants-2005_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06903090B2

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