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Hydrochloric Acid → HCID 21941358、化合物

HRID 2216631
ノート
印刷プレビュー

反応式

HRID 2216631 の反応式
Cl.CO.[N:4]1[N:8]2[CH2:9][CH2:10][NH:11][CH2:12][C:7]2=[CH:6][C:5]=1[CH2:13][OH:14].CS[C:17]1[S:18][CH2:19][CH2:20][N:21]=1>C(OCC)C>[S:18]1[CH2:19][CH2:20][N:21]=[C:17]1[N:11]1[CH2:10][CH2:9][N:8]2[N:4]=[C:5]([CH2:13][OH:14])[CH:6]=[C:7]2[CH2:12]1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 887MethanolHCID 883244,5-Dihydro-2-(methylthio)thiazoleHCID 21941456(4,5,6,7-Tetrahydropyrazolo[1,5-A]pyrazin-2-YL)methanol

生成物 1

HCID 21941358HCID 21941358、化合物

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

Hydrogen chloride (2 mol/l) solution in diethyl ether (0.7 ml) was added to the methanol (20 ml) solution of (4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazin-2-yl)-methanol (1.08 g) and 2-methylsulfanyl-4,5-dihydrothiazole (1.03 g). The reaction mixture was refluxed for 4 days. The mixture was quenched with small amount of saturated potassium carbonate solution, dried (MgSO4) and filtered. The filtrate was concentrated under reduced pressure. The residue was applied to silica-gel column chromatography, then the column was eluted with 10% methanol in chloroform. The titled compound was obtained as a white solid (1.49 g, 89%).

後処理

  1. temperatureThe reaction mixture was refluxed for 4 days
  2. customThe mixture was quenched with small amount of saturated potassium carbonate solution
  3. dry with materialdried (MgSO4)
  4. filtrationfiltered
  5. concentrationThe filtrate was concentrated under reduced pressure
  6. washthe column was eluted with 10% methanol in chloroform

出典と根拠

ORDレコード
ord-91f06c49b5194ce2840b3e9ca637f0c1
出典データセット
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07112582B2

反応ノート

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