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Hydrochloric Acid → 6-Pentyl-6,9-dihydro-5H-[1,2,4]triazolo[3,4-i]purin-5-one

HRID 2374305
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HRID 2374305 반응식
C([N:8]1[C:16]2[C:15]3=[N:17][N:18]=[CH:19][N:14]3[C:13](=[O:20])[N:12]([CH2:21][CH2:22][CH2:23][CH2:24][CH3:25])[C:11]=2[N:10]=[CH:9]1)C1C=CC=CC=1.Cl>C(O)(=O)C.[OH-].[Pd+2].[OH-]>[CH2:21]([N:12]1[C:11]2[N:10]=[CH:9][NH:8][C:16]=2[C:15]2=[N:17][N:18]=[CH:19][N:14]2[C:13]1=[O:20])[CH2:22][CH2:23][CH2:24][CH3:25]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 313Hydrochloric AcidHCID 598538329-Benzyl-6-pentyl-6,9-dihydro-5H-[1,2,4]triazolo[3,4-i]purin-5-one

생성물 1

HCID 1359846986-Pentyl-6,9-dihydro-5H-[1,2,4]triazolo[3,4-i]purin-5-one수율 65.8%

시약·촉매·용매 2

HCID 9942167Palladium hydroxide촉매2회HCID 176Acetic Acid용매

실험 절차

To a mixture of 9-benzyl-6-pentyl-6,9-dihydro-5H-[1,2,4]triazolo[3,4-i]purin-5-one (0.25 g, 0.74 mmol) in acetic acid (20 mL) was added palladium hydroxide (0.20 g, 1.4 mmol) under N2. The mixture was shaken under H2 at 60 psi overnight. Since the reaction was not complete, more palladium hydroxide (0.2 g, 1.4 mmol) and concentrated HCl (1 mL) were added. The resulting mixture was shaken under H2 at 60 psi overnight. The reaction solution was filtered and the filtrate was concentrated under vacuum to provide the product as a white solid (0.12 g, 65.6%). LCMS calculated for C11H15N6O (M+H): 247.1; found: 247.1.

후처리

  1. stirringThe resulting mixture was shaken under H2 at 60 psi overnight
  2. filtrationThe reaction solution was filtered
  3. concentrationthe filtrate was concentrated under vacuum

출처 및 근거

ORD 기록
ord-53a61a0dd4e841bc9f9f4f37a0ff506f
출처 데이터셋
uspto-grants-2008_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07462624B2

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