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6-Amino-9-benzyl-2-(2-ethoxyethoxy)-8-methoxypurine → HCID 178467997, compound

HRID 2269065
Notes
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Reaction equation

HRID 2269065 reaction equation
[NH2:1][C:2]1[N:10]=[C:9]([O:11][CH2:12][CH2:13][O:14][CH2:15][CH3:16])[N:8]=[C:7]2[C:3]=1[N:4]=[C:5]([O:24]C)[N:6]2[CH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>Cl>[NH2:1][C:2]1[N:10]=[C:9]([O:11][CH2:12][CH2:13][O:14][CH2:15][CH3:16])[N:8]=[C:7]2[C:3]=1[N:4]=[C:5]([OH:24])[N:6]2[CH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 183326966-Amino-9-benzyl-2-(2-ethoxyethoxy)-8-methoxypurine

Product 1

HCID 178467997HCID 178467997, compoundYield 84%

Reagents, catalysts & solvents 1

HCID 313Hydrochloric AcidSolvent

Procedure

6-Amino-9-benzyl-2-(2-ethoxyethoxy)-8-methoxypurine (110 mg, 0.32 mmol) in concentrated hydrochloric acid (20 ml) was stirred at room temperature for 12 hours. The reaction mixture was evaporated in vacuo to dryness and then 28% aqueous ammonia was added thereto. The resulting crystals were filtered to give the subject compound (88 mg, yield 84%).

Workup

  1. customThe reaction mixture was evaporated in vacuo to dryness
addition
28% aqueous ammonia was added
  • filtrationThe resulting crystals were filtered
  • Sources & evidence

    ORD record
    ord-6d7a7f1911c446f5bfbbf3b8857b60ab
    Source dataset
    uspto-grants-2001_12
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US06329381B1

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes