Tert-Butylamine → N-tert-butyl-4-[1-(4-methoxybenzyl)-3-(3-nitrophenyl)-1H-pyrazol-4-yl]pyridin-2-amine

HRID 1843645

반응식

HRID 1843645 반응식
[CH3:1][O:2][C:3]1[CH:30]=[CH:29][C:6]([CH2:7][N:8]2[CH:12]=[C:11]([C:13]3[CH:18]=[CH:17][N+:16]([O-])=[CH:15][CH:14]=3)[C:10]([C:20]3[CH:25]=[CH:24][CH:23]=[C:22]([N+:26]([O-:28])=[O:27])[CH:21]=3)=[N:9]2)=[CH:5][CH:4]=1.[C:31]([NH2:35])([CH3:34])([CH3:33])[CH3:32].C1(C)C=CC(S(OS(C2C=CC(C)=CC=2)(=O)=O)(=O)=O)=CC=1>FC(C1C=CC=CC=1)(F)F.ClCCl>[C:31]([NH:35][C:15]1[CH:14]=[C:13]([C:11]2[C:10]([C:20]3[CH:25]=[CH:24][CH:23]=[C:22]([N+:26]([O-:28])=[O:27])[CH:21]=3)=[N:9][N:8]([CH2:7][C:6]3[CH:29]=[CH:30][C:3]([O:2][CH3:1])=[CH:4][CH:5]=3)[CH:12]=2)[CH:18]=[CH:17][N:16]=1)([CH3:34])([CH3:33])[CH3:32]

참가 물질

6

실험 절차

580 mg (1.44 mmol) of 4-[1-(4-methoxybenzyl)-3-(3-nitrophenyl)-1H-pyrazol-4-yl]pyridine 1-oxide were suspended in a mixture of 16 ml of trifluoromethylbenzene and 4 ml of dry dichloromethane and 756 μl of tert-butylamine were added. At 0° C. 936 mg (7.2 mmol) of p-toluensulfonic anhydride were added. After 6 hours under stirring in the same conditions the solvent was removed under reduced pressure, the residue partitioned between dichloromethane and water, the organic layer dried over sodium sulphate and evaporated. The crude was then purified by flash-chromatography on a silica gel column (CH2Cl2-CH3COCH3 19/1), giving 500 mg (75%) of the title compound.

후처리

  1. additionwere added
  2. customAt 0° C
  3. customwas removed under reduced pressure
  4. customthe residue partitioned between dichloromethane and water
  5. dry with materialthe organic layer dried over sodium sulphate
  6. customevaporated
  7. customThe crude was then purified by flash-chromatography on a silica gel column (CH2Cl2-CH3COCH3 19/1)

출처 및 근거

ORD 기록
ord-9fa05e8f432c4aaaac93fd42ead53fa4
출처 데이터셋
uspto-grants-2015_02
특허 번호
US08946250B2

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