Sodium Hydroxide → HCID 23158505, compound

HRID 2036319Notes

Reaction equation

HRID 2036319 reaction equation
[H-].[Al+3].[Li+].[H-].[H-].[H-].[CH2:7]([O:11][C:12]1[N:20]=[C:19]2[C:15]([N:16]=[CH:17][N:18]2[CH2:21][CH2:22][O:23][C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=2[C:30](OC)=[O:31])=[C:14]([NH2:34])[N:13]=1)[CH2:8][CH2:9][CH3:10].[OH-].[Na+]>C1COCC1>[CH2:7]([O:11][C:12]1[N:20]=[C:19]2[C:15]([N:16]=[CH:17][N:18]2[CH2:21][CH2:22][O:23][C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=2[CH2:30][OH:31])=[C:14]([NH2:34])[N:13]=1)[CH2:8][CH2:9][CH3:10]

Participants

5

Procedure

To a suspension of lithium aluminum hydride (74 mg, 1.9 mmol) in THF (10 ml) was added a solution of 2-butoxy-9-[2-(2-methoxycarbonylphenoxy)ethyl]adenine (500 mg, 1.4 mmol) obtained by Reference Example 5 in THF (2 ml) under ice-cooling, and the mixture was stirred at room temperature for 1 hour. 1N Aqueous sodium hydroxide solution was added thereto, followed by filtration through celite pad, and the filtrate was concentrated under reduced pressure to give 500 mg (1.4 mmol) of the titled compound as a white solid. Yield: 99%.

Workup

  1. temperaturecooling
  2. filtrationfollowed by filtration through celite pad
  3. concentrationthe filtrate was concentrated under reduced pressure

Sources & evidence

ORD record
ord-383e6e5e56424e139c31095498659e32
Source dataset
uspto-grants-2013_11
Patent number
US08575180B2

Reaction notes

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