Hydrazine hydrate (1:1) → O-{[4-amino-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinolin-2-yl]methyl}hydroxylamine

HRID 599394노트

반응식

HRID 599394 반응식
O.NN.[NH2:4][C:5]1[C:14]2[N:15]=[C:16]([CH2:22][O:23][N:24]3C(=O)C4C(=CC=CC=4)C3=O)[N:17]([CH2:18][CH:19]([CH3:21])[CH3:20])[C:13]=2[C:12]2[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=2[N:6]=1>C(O)C>[NH2:4][C:5]1[C:14]2[N:15]=[C:16]([CH2:22][O:23][NH2:24])[N:17]([CH2:18][CH:19]([CH3:20])[CH3:21])[C:13]=2[C:12]2[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=2[N:6]=1

참가 물질

4

반응물 2

HCID 24654Hydrazine hydrate (1:1)HCID 67052437HCID 67052437, 화합물

생성물 1

HCID 11414929O-{[4-amino-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinolin-2-yl]methyl}hydroxylamine수율 77.3%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Hydrazine hydrate (9 mL) was added to a suspension of 2-{[4-amino-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinolin-2-yl]methoxy}isoindole-1,3-dione (3.9 g) in ethanol (90 mL). The resulting solution was stirred at ambient temperature for 3 hours. The reaction mixture was filtered to remove a precipitate and the filter cake was washed with ethanol and dichloromethane. The filtrate was concentrated under reduced pressure, diluted with aqueous 1N hydrochloric acid (100 mL), and then washed sequentially with dichloromethane (2×50 mL) and ethyl acetate (1×50 mL). Analysis of the organic washes by LCMS indicated that they did not contain product. The aqueous acidic layer was made basic (˜pH 9) with solid sodium carbonate and then extracted sequentially with dichloromethane (1×100 mL), ethyl acetate (1×100 mL), and dichloromethane (1×100 mL). The combined organic extracts were dried over magnesium sulfate, filtered and then concentrated under reduced pressure to provide 2.07 g of O-{[4-amino-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinolin-2-yl]methyl}hydroxylamine as a tan foam.

후처리

  1. filtrationThe reaction mixture was filtered
  2. customto remove a precipitate
  3. washthe filter cake was washed with ethanol and dichloromethane
  4. concentrationThe filtrate was concentrated under reduced pressure
  5. additiondiluted with aqueous 1N hydrochloric acid (100 mL)
  6. washwashed sequentially with dichloromethane (2×50 mL) and ethyl acetate (1×50 mL)
  7. extractionextracted sequentially with dichloromethane (1×100 mL), ethyl acetate (1×100 mL), and dichloromethane (1×100 mL)
  8. dry with materialThe combined organic extracts were dried over magnesium sulfate
  9. filtrationfiltered
  10. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-42a057faa4c145a4bfc4cacecb2da938
출처 데이터셋
uspto-grants-2011_03
특허 번호
US07897767B2

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