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Hydrogen Bromide → 3-Nitro-6,7-dihydro-5H-cyclopenta[b]pyridin-4-ol

HRID 924400
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HRID 924400 반응식
C[O:2][C:3]1[C:8]([N+:9]([O-:11])=[O:10])=[CH:7][N:6]=[C:5]2[CH2:12][CH2:13][CH2:14][C:4]=12.Br>CC(O)=O>[N+:9]([C:8]1[C:3]([OH:2])=[C:4]2[CH2:14][CH2:13][CH2:12][C:5]2=[N:6][CH:7]=1)([O-:11])=[O:10]
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참가 물질

4

반응물 2

HCID 260Hydrogen BromideHCID 867266844-Methoxy-3-nitro-6,7-dihydro-5H-cyclopenta[b]pyridine

생성물 1

HCID 1785267573-Nitro-6,7-dihydro-5H-cyclopenta[b]pyridin-4-ol

시약·촉매·용매 1

HCID 176Acetic Acid용매

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온도
130 °C

실험 절차

A mixture of 4-methoxy-3-nitro-6,7-dihydro-5H-cyclopenta[b]pyridine (1.535 g, 7.905 mmol) in AcOH (2.6 mL) was treated with 48% aq. HBr (2.6 mL, 23 mmol). The flask was sealed and heated at 130° C. for 40 min. then allowed to cool. The mixture was then concentrated under reduced pressure and the residue was neutralized to pH=7-8 using 50% NaOH in a cold bath. The mixture was then concentrated under reduced pressure and the residue was diluted with MeOH and THF, dried, filtered and concentrated to give the sub-title compound as a light brown powder. LCMS calc. for C8H9N2O3(M+H)+: m/z=181.3. Found: 181.2.

후처리

  1. customThe flask was sealed
  2. temperatureto cool
  3. concentrationThe mixture was then concentrated under reduced pressure
  4. concentrationThe mixture was then concentrated under reduced pressure
  5. additionthe residue was diluted with MeOH and THF
  6. customdried
  7. filtrationfiltered
  8. concentrationconcentrated

출처 및 근거

ORD 기록
ord-b82360d12a5f4568926b52503c412d5e
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09278950B2

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