1-Propanol → 1H-Pyrrolo[2,3-b]pyridine-3-carboxylic acid, 1-(1,1-dimethylethyl)-5-nitro-, propyl ester

HRID 217955노트

반응식

HRID 217955 반응식
[C:1]([N:5]1[C:9]2=[N:10][CH:11]=[C:12]([N+:14]([O-:16])=[O:15])[CH:13]=[C:8]2[C:7]([C:17]#N)=[CH:6]1)([CH3:4])([CH3:3])[CH3:2].C1(C)C=CC(S(O)(=O)=[O:26])=CC=1.[CH2:30]([OH:33])[CH2:31][CH3:32]>COC(C)(C)C>[CH2:30]([O:33][C:17]([C:7]1[C:8]2[C:9](=[N:10][CH:11]=[C:12]([N+:14]([O-:16])=[O:15])[CH:13]=2)[N:5]([C:1]([CH3:2])([CH3:3])[CH3:4])[CH:6]=1)=[O:26])[CH2:31][CH3:32]

참가 물질

5

실험 절차

To a suspension of 5.0 g (20.47 mmol) of 1-tert-butyl-5-nitro-1H-pyrrolo[2,3-b]pyridine-3-carbonitrile in 125 mL of n-propanol, 7.78 g of p-toluensulfonic acid were added under stirring. The mixture was heated at reflux for 40 hours and then it was cooled to room temperature and diluted with 70 mL of tert-butyl methyl ether. The precipitate was filtered off and the clear filtrate was concentrated under vacuum to a small volume (about 40-50 mL). The suspension was cooled to −5/0° C. and kept at this temperature for 2 hours. The solid was filtered, washed with 20 mL of 1:1 mixture of n-propanol and tert-butyl methyl ether and dried to afford 5.50 g of the title compound as a cream-colored solid.

후처리

  1. additionwere added
  2. temperatureThe mixture was heated
  3. temperatureat reflux for 40 hours
  4. filtrationThe precipitate was filtered off
  5. concentrationthe clear filtrate was concentrated under vacuum to a small volume (about 40-50 mL)
  6. temperatureThe suspension was cooled to −5/0° C.
  7. filtrationThe solid was filtered
  8. washwashed with 20 mL of 1:1 mixture of n-propanol and tert-butyl methyl ether
  9. customdried

출처 및 근거

ORD 기록
ord-668c62337f25451aae9f96859c6d4982
출처 데이터셋
uspto-grants-2012_06
특허 번호
US08198298B2

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