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2-Amino-3,5-dinitropyridine → 5-Nitropyridine-2,3-diamine

HRID 343789
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HRID 343789 반응식
[NH2:1][C:2]1[C:7]([N+:8]([O-])=O)=[CH:6][C:5]([N+:11]([O-:13])=[O:12])=[CH:4][N:3]=1>CO>[NH2:1][C:2]1[C:7]([NH2:8])=[CH:6][C:5]([N+:11]([O-:13])=[O:12])=[CH:4][N:3]=1
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참가 물질

3

반응물 1

HCID 5043402-Amino-3,5-dinitropyridine

생성물 1

HCID 34801515-Nitropyridine-2,3-diamine수율 80.6%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a suspension of 61 (1.617 g, 8.79 mmol) in MeOH (75 mL) was added 20% aq. (NH4)2S (15 mL, 44 mmol) dropwise at room temperature with stirring. The resulting dark-red solution was stirred at room temperature for 0.5 h, then refluxed for 0.5 h, then cooled to room temperature. The resulting mixture was filtered. The filtrate was concentrated to about 30 mL and cooled in ice-water. The precipitate was filtered, washed with cooled EtOH (2×5 mL), and dried to give 1.092 g (80%) of 62 as a deep red powder, mp 260°-2° C.(dec) (Lit., 260° C., Chemical Abstracts 65:3826 (1966)). 1H NMR (DMSO-d6): 5.311 (s, 2H), 6.984 (s, 2H), 7.342 (d, 1H, J=2.2), 8.171 (d, 1H, J=2.2).

후처리

  1. stirringThe resulting dark-red solution was stirred at room temperature for 0.5 h
  2. temperaturerefluxed for 0.5 h
  3. filtrationThe resulting mixture was filtered
  4. concentrationThe filtrate was concentrated to about 30 mL
  5. temperaturecooled in ice-water
  6. filtrationThe precipitate was filtered
  7. washwashed with cooled EtOH (2×5 mL)
  8. customdried

출처 및 근거

ORD 기록
ord-f27a0ad026ef409ca1658d902d618ec0
출처 데이터셋
uspto-grants-1999_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05863916

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