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Ethyl 5-cyanoindole-2-carboxylate → 5-Aminomethyl-1H-indole-2-carboxylic acid ethyl ester

HRID 843998
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HRID 843998 반응식
[CH2:1]([O:3][C:4]([C:6]1[NH:7][C:8]2[C:13]([CH:14]=1)=[CH:12][C:11]([C:15]#[N:16])=[CH:10][CH:9]=2)=[O:5])[CH3:2]>C(Cl)Cl>[CH2:1]([O:3][C:4]([C:6]1[NH:7][C:8]2[C:13]([CH:14]=1)=[CH:12][C:11]([CH2:15][NH2:16])=[CH:10][CH:9]=2)=[O:5])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 4714953Ethyl 5-cyanoindole-2-carboxylate

생성물 1

HCID 252537375-Aminomethyl-1H-indole-2-carboxylic acid ethyl ester

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A solution of 5-Cyano-1H-indole-2carboxylic acid ethyl ester (1.8 grams, 8.4 mmole) and Bu4N+BH3− in methylene chloride (80 ml) was refluxed for 4 hours. The mixture was concentrated to a brown oil which was dissolved in 10% hydrochloric acid (50 ml) and refluxed for 1 hour. The mixture was extracted with ethyl acetate (discarded) and the pH was neutralized. The aqueous was extracted with ethyl acetate. The combined extracts were dried over Na2SO4, filtered, and concentrated to give a solid. (0.920 g). MW 218.258; MS (m/e) 218 (M+).

후처리

  1. concentrationThe mixture was concentrated to a brown oil which
  2. dissolutionwas dissolved in 10% hydrochloric acid (50 ml)
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • temperaturerefluxed for 1 hour
  • extractionThe mixture was extracted with ethyl acetate (discarded)
  • extractionThe aqueous was extracted with ethyl acetate
  • dry with materialThe combined extracts were dried over Na2SO4
  • filtrationfiltered
  • concentrationconcentrated
  • customto give a solid
  • 출처 및 근거

    ORD 기록
    ord-92f6329b118840dd893056102cb4afaf
    출처 데이터셋
    uspto-grants-2002_04
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06380218B1

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