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Thionyl Chloride → HCID 136360831, 화합물

HRID 1487432
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HRID 1487432 반응식
O[CH2:2][C:3]1[C:4]([C:11]2[NH:12][CH:13]=[CH:14][N:15]=2)=[C:5]([OH:10])[C:6]([CH3:9])=[N:7][CH:8]=1.S(Cl)([Cl:18])=O>C1(C)C=CC=CC=1>[ClH:18].[Cl:18][CH2:2][C:3]1[C:4]([C:11]2[NH:12][CH:13]=[CH:14][N:15]=2)=[C:5]([OH:10])[C:6]([CH3:9])=[N:7][CH:8]=1
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참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 1355326695-(Hydroxymethyl)-4-(1H-imidazol-2-yl)-2-methylpyridin-3-ol

생성물 1

HCID 136360831HCID 136360831, 화합물

시약·촉매·용매 1

HCID 1140Toluene용매

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온도
0 °C

실험 절차

5-(hydroxymethyl)-4-(1H-imidazol-2-yl)-2-methylpyridin-3-ol (5.1 g, 25 mmol) was suspended in toluene (100 mL) and thionyl chloride (25 mL) was added. The suspension was heated to reflux for 2 h, cooled to 0° C. and filtered. The title compound was obtained as brown solid (Purity by NMR: 70-80%) and was used without further purification in the next step.

후처리

  1. temperatureThe suspension was heated
  2. temperatureto reflux for 2 h
  3. filtrationfiltered

출처 및 근거

ORD 기록
ord-58b7f2a8e55a4b9a9186cc9ad17e9065
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09428533B2

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