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Hydrazine hydrate (1:1) → HCID 59442111, 화합물

HRID 1014175
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HRID 1014175 반응식
[CH3:1][C:2]1[CH:3]=[C:4]([C:11]2[CH2:16][N:15]([CH2:17][CH2:18][CH3:19])[CH2:14][CH2:13][CH:12]=2)[CH:5]=[CH:6][C:7]=1[N+:8]([O-])=O.O.NN>CO.[Fe](Cl)(Cl)Cl>[CH3:1][C:2]1[CH:3]=[C:4]([C:11]2[CH2:16][N:15]([CH2:17][CH2:18][CH3:19])[CH2:14][CH2:13][CH:12]=2)[CH:5]=[CH:6][C:7]=1[NH2:8]
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참가 물질

5

반응물 2

HCID 24654Hydrazine hydrate (1:1)HCID 59441646HCID 59441646, 화합물

생성물 1

HCID 59442111HCID 59442111, 화합물수율 82%

시약·촉매·용매 2

HCID 24380Iron chloride (FeCl3)촉매HCID 887Methanol용매

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온도
64 °C

실험 절차

To 5-(3-methyl-4-nitrophenyl)-1-propyl-1,2,3,6-tetrahydropyridine (5.0 g, 19.2 mmol) in MeOH (100 mL) was added iron (III) chloride (0.93 g, 5.8 mmol, Aldrich) and activated carbon (1.0 g, Aldrich). The reaction mixture was stirred at 64° C. for 20 min before the dropwise addition of hydrazine hydrate (11.5 mL, 230.8 mmol, Aldrich) over 5 min. The reaction was kept stirring at 64° C. for additional 5 h. Filtration removed the solids and the filtrate was concentrated and purified via chromatography on SiO2 (0-10% 2 M NH3 in MeOH/DCM) to afford 2-methyl-4-(1-propyl-1,2,5,6-tetrahydro-3-pyridinyl)aniline (3.6 g, 82% yield.) 1H NMR (400 MHz, CDCl3) δ ppm 0.94 (t, J=7.4 Hz, 3 H), 1.57-1.67 (m, 2 H), 2.16 (s, 3 H), 2.33 (tt, J=5.9, 2.9 Hz, 2 H), 2.44-2.50 (m, 2 H), 2.59 (t, J=5.8 Hz, 2 H), 3.29 (q, J=2.0 Hz, 2 H), 3.58 (s, 2 H), 5.96 (dq, J=3.9, 2.0 Hz, 1 H), 6.61 (d, J=7.9 Hz, 1 H), 7.02-7.06 (m, 2 H).

후처리

  1. filtrationFiltration
  2. customremoved the solids
  3. concentrationthe filtrate was concentrated
  4. custompurified via chromatography on SiO2 (0-10% 2 M NH3 in MeOH/DCM)

출처 및 근거

ORD 기록
ord-301a27e46a994670878b6f7789bc2a83
출처 데이터셋
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07981903B2

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