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

HRID 1499441
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HRID 1499441 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 48% aq. HBr (2.6 mL, 23 mmol). The flask containing the mixture was sealed and heated at 130° C. for 40 min., then allowed to cool. The resulting mixture was concentrated under reduced pressure, the residue was neutralized to pH=7-8 using 50% NaOH with cooling. After further concentrating, the residue was diluted with MeOH and THF, dried, filtered and concentrated to give the crude sub-title compound as light brown powder, which was used without further purification. LCMS calc. for C8H9N2O3 (M+H)+: m/z=181.1. Found: 181.2.

후처리

  1. additionThe flask containing the mixture
  2. customwas sealed
  3. temperatureto cool
  4. concentrationThe resulting mixture was concentrated under reduced pressure
  5. temperaturewith cooling
  6. concentrationAfter further concentrating
  7. additionthe residue was diluted with MeOH and THF
  8. customdried
  9. filtrationfiltered
  10. concentrationconcentrated

출처 및 근거

ORD 기록
ord-8c95c78d08464217bad2602988bc48bd
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09200004B2

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