6-nitro-1H-indole-2-carbonitrile → 6-Amino-1H-indole-2-carbonitrile

HRID 503382노트

반응식

HRID 503382 반응식
[N+:1]([C:4]1[CH:12]=[C:11]2[C:7]([CH:8]=[C:9]([C:13]#[N:14])[NH:10]2)=[CH:6][CH:5]=1)([O-])=O>[Ni].CCO>[NH2:1][C:4]1[CH:12]=[C:11]2[C:7]([CH:8]=[C:9]([C:13]#[N:14])[NH:10]2)=[CH:6][CH:5]=1

참가 물질

4

반응물 1

HCID 574701946-nitro-1H-indole-2-carbonitrile

생성물 1

HCID 451170156-Amino-1H-indole-2-carbonitrile수율 49%

시약·촉매·용매 2

HCID 935Nickel촉매HCID 702Ethanol용매

실험 절차

A mixture of 6-nitro-1H-indole-2-carbonitrile (2.5 g, 13 mmol) and Raney Nickel (500 mg) in EtOH (50 mL) was stirred at room temperature under H2 (1 atm) for 1 h. Raney Nickel was removed via filtration and the filtrate was evaporated under reduced pressure to give a residue, which was purified by column chromatograpy on silica get to give 6-amino-1H-indole-2-carbonitrile (1.0 g, 49%). 1H NMR (DMSO-d6) δ 12.75 (br s, 1H), 7.82 (d, J=8 Hz, 1H), 7.57 (s, 1H), 7.42 (s, 1H), 7.15 (d, J=8 Hz, 1H); MS (ESI) m/e (M+H+) 158.2.

후처리

  1. customRaney Nickel was removed via filtration
  2. customthe filtrate was evaporated under reduced pressure
  3. customto give a residue, which
  4. customwas purified by column chromatograpy on silica
  5. customget

출처 및 근거

ORD 기록
ord-ce56e4c69743430ba06e3e01e4296936
출처 데이터셋
uspto-grants-2010_08
특허 번호
US07776905B2

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