Adenosine → HCID 3001844, compound

HRID 1006407Notes

Reaction equation

HRID 1006407 reaction equation
C1N(/C=C2/CC/2CO)C2N=C(N)N=C(O)C=2N=1.[C@@H:18]1([N:27]2[C:36]3[N:35]=[CH:34][N:33]=[C:31]([NH2:32])[C:30]=3[N:29]=[CH:28]2)O[C@H:23]([CH2:24][OH:25])[C@@H:21](O)[C@H:19]1O>ClCCl.CO>[CH2:21]1[C@@H:23]([CH2:24][OH:25])/[C:19]/1=[CH:18]\[N:27]1[C:36]2[N:35]=[CH:34][N:33]=[C:31]([NH2:32])[C:30]=2[N:29]=[CH:28]1

Participants

4

Procedure

A suspension of racemic synadenol (1, B=adenin-N9-yl, 200 mg, 0.92 mmol) from Example 5 in 0.05 M Na2HPO4 (pH 7.5, 100 mL) was briefly sonicated. Adenosine deaminase from calf intestine (Type II, Sigma Chemical Co., St. Louis, Mo., 30 mg, 45 units) was added and the mixture was stirred at room temperature. The progress of the reaction was followed by TLC in dichloromethane—methanol (9:1). The deamination stopped after 72 h and the ratio of synadenol (1, B=adenin-N9-yl): synhypoxanthol (1, B=hypoxanthin-N9-yl) was 7:3 as determined by UV spectrophotometry of the eluted spots. Addition of another two portions of enzyme (30 mg every 24 h) did not improve this ratio. The mixture was lyophilized and the resultant product was sonicated with several portions of dichloromethane—methanol (1:1, first 100 mL and then 40 mL) until no UV absorption was detectable in the solvent. The filtrate and washings were combined and evaporated. The residue was adsorbed on silica gel (4 g) and loaded on a column made of the same material. Chromatography using dichloromethane—methanol (9:1) as an eluent afforded (R)-(−)-synadenol (1, B=adenin-N9-yl), 135 mg, 66.5%), [α]25D 59.1° (c 0.04, MeOH) and elution with dichloromethane—methanol (4:1) gave (S)-(+)-synhypoxanthol (1, B=hypoxanthin-N9-yl), 85 mg, [α]25D 91.8° (c 0.1, MeOH).

Workup

  1. customwas briefly sonicated
  2. additionAddition of another two portions of enzyme (30 mg every 24 h)
  3. custom40 mL) until no UV absorption
  4. customevaporated

Sources & evidence

ORD record
ord-eab8c5d72d5749cbaac18b4c7755984d
Source dataset
uspto-grants-2004_09
Patent number
US06790841B2

Reaction notes

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