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Hydrochloric Acid → 5-(p-Tolyl)-5,6,7,8-tetrahydroimidazo[1,5-a]pyridine hydrochloride

HRID 22542
ノート
印刷プレビュー

反応式

HRID 22542 の反応式
O[CH2:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[N:14]3[CH:15]=[N:16][CH:17]=[C:13]3[CH:12]=[CH:11][CH:10]=2)=[CH:5][CH:4]=1.[H][H].[ClH:20]>C(O)C.[Pd]>[ClH:20].[C:3]1([CH3:2])[CH:8]=[CH:7][C:6]([CH:9]2[N:14]3[CH:15]=[N:16][CH:17]=[C:13]3[CH2:12][CH2:11][CH2:10]2)=[CH:5][CH:4]=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 3

HCID 313Hydrochloric AcidHCID 136494325-(p-Hydroxymethylphenyl)imidazo[1,5-a]pyridineHCID 178418361HCID 178418361、化合物

生成物 1

HCID 136882175-(p-Tolyl)-5,6,7,8-tetrahydroimidazo[1,5-a]pyridine hydrochloride

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 702Ethanol溶媒

実験手順

A solution of 0.36 g of 5-(p-hydroxymethylphenyl)imidazo[1,5-a]pyridine in 25 ml of ethanol and 6.4 ml of concentrated hydrochloric acid is hydrogenated with 0.15 g of 10% palladium on charcoal at 40 psi of hydrogen and 60° for 4 h. The reaction mixture is filtered and evaporated and the residue is partitioned between methylene chloride and sodium bicarbonate solution. The organic phase is dried over sodium sulfate and evaporated to an oil which is purified by preparative layer chromatography on silica with ethyl acetate. The hydrochloride salt is prepared in acetone with 1.1 molar equivalents of ethereal hydrogen chloride to yield the title compound, m.p. 173°-175°.

後処理

  1. filtrationThe reaction mixture is filtered
  2. customevaporated
  3. customthe residue is partitioned between methylene chloride and sodium bicarbonate solution
  4. dry with materialThe organic phase is dried over sodium sulfate
  5. customevaporated to an oil which
  6. customis purified by preparative layer chromatography on silica with ethyl acetate

出典と根拠

ORDレコード
ord-0a61a88f7fe74066acb7c5361000e070
出典データセット
uspto-grants-1995_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05428160

反応ノート

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