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Ammonia → 1-(3-aminopropyl)-1H-imidazo[4,5-c]quinoline-4-amine

HRID 1108632
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HRID 1108632 반응식
[NH2:1][CH2:2][CH2:3][CH2:4][N:5]1[C:17]2[C:16]3[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=3[N:10]=[C:9](Cl)[C:8]=2[N:7]=[CH:6]1.[NH3:19]>CO>[NH2:1][CH2:2][CH2:3][CH2:4][N:5]1[C:17]2[C:16]3[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=3[N:10]=[C:9]([NH2:19])[C:8]=2[N:7]=[CH:6]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 222AmmoniaHCID 177767961-(3-aminopropyl)-4-chloro-1H-imidazo[4,5-c]quinoline

생성물 1

HCID 187839731-(3-aminopropyl)-1H-imidazo[4,5-c]quinoline-4-amine

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

14 mg (0.0536 mmol) of 1-(3-aminopropyl)-4-chloro-1H-imidazo[4,5-c]quinoline, 5 ml of methanol and 3 ml of liquid ammonia were stirred in an autoclave overnight at 150° C. under heating. The reaction mixture was concentrated under reduced pressure and 0.3 ml of a 1N sodium hydroxide solution was added to the residue. The precipitate thus formed was collected by filtration to obtain 8 mg (0.0331 ml) of 1-(3-aminopropyl)-1H-imidazo[4,5-c]quinoline-4-amine shown below. ##STR38## The physicochemical data of this compound was in agreement with the compound of Example 5.

후처리

  1. temperatureunder heating
  2. concentrationThe reaction mixture was concentrated under reduced pressure and 0.3 ml of a 1N sodium hydroxide solution
  3. additionwas added to the residue
  4. customThe precipitate thus formed
  5. filtrationwas collected by filtration

출처 및 근거

ORD 기록
ord-402ea26c54de4db38548a53845d6f89d
출처 데이터셋
uspto-grants-2000_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06069149

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