Hydrochloric Acid → HCID 20135762, 화합물

HRID 580145노트

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HRID 580145 반응식
[CH2:1]([N:3]([CH2:23][CH3:24])[CH2:4][CH2:5][CH2:6][NH:7][C:8]1[C:16]2[C:11](=[C:12]([N+:20]([O-])=O)[CH:13]=[C:14]([N+:17]([O-])=O)[CH:15]=2)[NH:10][N:9]=1)[CH3:2].CO.O.Cl>[Fe].C(Cl)(Cl)Cl>[CH2:23]([N:3]([CH2:1][CH3:2])[CH2:4][CH2:5][CH2:6][NH:7][C:8]1[C:16]2[C:11](=[C:12]([NH2:20])[CH:13]=[C:14]([NH2:17])[CH:15]=2)[NH:10][N:9]=1)[CH3:24]

참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 887MethanolHCID 962WaterHCID 20135777N~3~-(5,7-Dinitro-1H-indazol-3-yl)-N~1~,N~1~-diethylpropane-1,3-diamine

생성물 1

HCID 20135762HCID 20135762, 화합물수율 22.6%

시약·촉매·용매 2

HCID 23925Iron촉매HCID 6212Chloroform용매

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온도
70 °C

실험 절차

A mixture consisting of 9.0 g of the 3-(3-diethylaminopropylamino)-5,7-dinitroindazole, 18 g of iron powder, 60 ml of methyl alcohol, 30 ml of water and 3 ml of hydrochloric acid was stirred for 1.5 hours at 70° C. After cooling, the mixture was filtered, and the pH of the filtrate was adjusted to 11 with an aqueous potassium carbonate solution. The filtrate was extracted three times with 50 ml of ethyl acetate. The ethyl acetate layer was washed with water and dried over anhydrous sodium sulfate. Then, ethyl acetate was removed under reduced pressure. The residue thus obtained was subjected to an alumina-column chromatography(alumina: 200 g) using chloroform as the developing solvent to give 1.67 g of 3-(3-diethylaminopropylamino)-5,7-diaminoindazole having the following analytical values in a yield of 22%.

후처리

  1. temperatureAfter cooling
  2. filtrationthe mixture was filtered
  3. extractionThe filtrate was extracted three times with 50 ml of ethyl acetate
  4. washThe ethyl acetate layer was washed with water
  5. dry with materialdried over anhydrous sodium sulfate
  6. customThen, ethyl acetate was removed under reduced pressure
  7. customThe residue thus obtained

출처 및 근거

ORD 기록
ord-24ad1db860ad4ff0953e39622fb2551d
출처 데이터셋
uspto-grants-1988_06
특허 번호
US04751302

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