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HCID 178423389, 화합물 → 6-Methylquinolin-3-amine

HRID 430549
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HRID 430549 반응식
[CH3:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[CH:7][C:6]([N+:12]([O-])=O)=[C:5]2O>[Pt].C(O)C.[OH-].[NH4+]>[NH2:12][C:6]1[CH:7]=[N:8][C:9]2[C:4]([CH:5]=1)=[CH:3][C:2]([CH3:1])=[CH:11][CH:10]=2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 178423389HCID 178423389, 화합물

생성물 1

HCID 221488796-Methylquinolin-3-amine수율 64.5%

시약·촉매·용매 3

HCID 23939Platinum촉매HCID 702Ethanol용매HCID 14923Ammonium Hydroxide용매

실험 절차

Catalyst (0.10 g of 10% platinum on carbon) was added to a solution of 6-methyl-3-nitroquinolin-4-ol (1 g) in ethanol (25 mL) and ammonium hydroxide (0.5 mL). The mixture was reduced on a Parr apparatus at ambient temperature under a hydrogen atmosphere. The reaction mixture was filtered to remove the catalyst and then concentrated under vacuum. The residue was combined with water and heated. Hydrochloric acid was added dropwise until all of the solid had dissolved. Activated carbon was added to the solution. The mixture was filtered. Hydrochloric acid (2 mL of 12N) was added to the filtrate. This recrystallization was run three times to provide 0.50 g of 3-amino-6-methylquinolin-+4ol hydrochloride, m.p. >310° C. Analysis: Calculated for C10H10N2O.HCl: % C, 57.02; % H, 5.26; % N, 13.30; Found: % C, 56.92; % H, 5.16; % N, 13.24.

후처리

  1. customwas reduced on a Parr apparatus at ambient temperature under a hydrogen atmosphere
  2. filtrationThe reaction mixture was filtered
  3. customto remove the catalyst
  4. concentrationconcentrated under vacuum
  5. temperatureheated
  6. additionHydrochloric acid was added dropwise until all of the solid
  7. dissolutionhad dissolved
  8. additionActivated carbon was added to the solution
  9. filtrationThe mixture was filtered
  10. additionHydrochloric acid (2 mL of 12N) was added to the filtrate
  11. customThis recrystallization

출처 및 근거

ORD 기록
ord-dd1ae662cb8d46e7813abd06ae707f50
출처 데이터셋
uspto-grants-2001_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06323200B1

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