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p-Toluenesulfonic acid → 6-Amino-1,3-dihydro-2H-indol-2-one

HRID 857434
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HRID 857434 반응식
C1[N:5]([CH2:6][O:7]CCO)[C:4]2NC(N)=[N:13][C:14](=O)[C:3]=2N=1.[C:17]1(C)[CH:22]=CC(S(O)(=O)=O)=[CH:19][CH:18]=1>C(O)C>[NH2:13][C:14]1[CH:3]=[C:4]2[C:18]([CH2:19][C:6](=[O:7])[NH:5]2)=[CH:17][CH:22]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6101p-Toluenesulfonic acidHCID 178508935HCID 178508935, 화합물

생성물 1

HCID 5905386-Amino-1,3-dihydro-2H-indol-2-one수율 3,626.2%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

2,4-dinitrophenylacetic acic (10 g; 44 mmol) was dissolved in ethanol (200 mL) and purged with N2. 10% Pd/C (400 mg) was added and the reaction hydrogenated at 45 psi for 2 hours. The reacton was then transferred to a RBF and p-toluenesulfonic acid (150 mg) was added and the reaction heated at reflux overnight. The reaction was then filtered through celite to remove catalyst and concentrated. The product crashed out and was filtered as tan crystals 4.68 g (72% yield). 1H NMR (DMSO-d6, 400 MHz) δ 3.20 (s, 2H), 4.97 (br s, 2H), 6.07 (m, 2H), 6.76 (d, J=8.7 Hz; 1H), 10.05 (s, 1H); HPLC ret. time: 2.123 min. LRMS (M+) 148.7.

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후처리

  1. custompurged with N2
  2. addition10% Pd/C (400 mg) was added
  3. customthe reaction hydrogenated at 45 psi for 2 hours
  4. additionwas added
  5. temperaturethe reaction heated
  6. temperatureat reflux overnight
  7. filtrationThe reaction was then filtered through celite
  8. customto remove catalyst
  9. concentrationconcentrated

출처 및 근거

ORD 기록
ord-a16fe0d064d14fdfa1c7c57ec5ec3b83
출처 데이터셋
uspto-grants-2006_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07145008B2

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