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

HRID 22542
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HRID 22542 반응식
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
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참가 물질

6

반응물 3

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

생성물 1

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

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

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°.

후처리

  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

출처 및 근거

ORD 기록
ord-0a61a88f7fe74066acb7c5361000e070
출처 데이터셋
uspto-grants-1995_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05428160

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