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Thionyl Chloride → HCID 10268183, 화합물

HRID 274362
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HRID 274362 반응식
[NH2:1][C:2]1[C:11]2[N:12]=[C:13]([CH2:19]O)[N:14]([CH2:15][CH:16]([CH3:18])[CH3:17])[C:10]=2[C:9]2[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=2[N:3]=1.S(Cl)([Cl:23])=O>CCOCC>[ClH:23].[Cl:23][CH2:19][C:13]1[N:14]([CH2:15][CH:16]([CH3:18])[CH3:17])[C:10]2[C:9]3[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=3[N:3]=[C:2]([NH2:1])[C:11]=2[N:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 9856687HCID 9856687, 화합물

생성물 1

HCID 10268183HCID 10268183, 화합물

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

4-Amino-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinoline-2-methanol (5.0 g; 0.0185 mol, Example 9) was added in small portions to vigorously stirred thionyl chloride (25 mL). The resulting mixture was stirred at room temperature overnight. The mixture was diluted with 100 mL of ether, and the solid was filtered from the mixture and dried thoroughly. The product was pure enough for further reactions. A sample was recrystallized from ethanol to give a pure product which melted with decomposition from 279°-292° C.

후처리

  1. filtrationthe solid was filtered from the mixture
  2. customdried thoroughly
  3. customA sample was recrystallized from ethanol
  4. customto give a pure product which
  5. custommelted with decomposition from 279°-292° C.

출처 및 근거

ORD 기록
ord-beb1da2dc7884979bf536906bda5e896
출처 데이터셋
uspto-grants-1995_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05389640

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