Diazomethane → HCID 22880806, compound

HRID 724800Notes

Reaction equation

HRID 724800 reaction equation
[I:1][C:2]1[N:3]=[C:4]([NH2:20])[C:5]2[N:6]=[CH:7][N:8]([C:18]=2[N:19]=1)[C@@H:9]1[O:17][C@H:14]([CH2:15][OH:16])[C@@H:12]([OH:13])[C@H:10]1[OH:11].O.O.[Sn](Cl)(Cl)(Cl)Cl.CO.[N+](=[CH2:32])=[N-]>COCCOC>[I:1][C:2]1[N:3]=[C:4]([NH2:20])[C:5]2[N:6]=[CH:7][N:8]([C:18]=2[N:19]=1)[C@@H:9]1[O:17][C@H:14]([CH2:15][OH:16])[C@@H:12]([OH:13])[C@H:10]1[O:11][CH3:32].[I:1][C:2]1[N:3]=[C:4]([NH2:20])[C:5]2[N:6]=[CH:7][N:8]([C:18]=2[N:19]=1)[C@@H:9]1[O:17][C@H:14]([CH2:15][OH:16])[C@@H:12]([O:13][CH3:32])[C@H:10]1[OH:11]

Participants

6

Procedure

1.2 g of 2-iodoadenosine was suspended in 150 ml of 1 mmol tin chloride dihydrate/methanol. 50 ml of 0.4-0.5M diazomethane in 1,2-dimethoxyethane was added with stirring. After stirring for one hour at room temperature, the reaction mixture was concentrated to dryness under reduced pressure. The resulting product was applied on ODS column and eluted with 40% (V/V) methanol in 0.1% (V/V) aqueous solution of TFA. First, 2-iodo-2'-O-methyladenosine (Compound 47) was eluted, and then 2-iodo-3'-O-methyladenosine (Compound 48) was eluted. Both fractions were concentrated to dryness to give 135 mg of Compound 47 and 56 mg of Compound 48.

Workup

  1. stirringAfter stirring for one hour at room temperature
  2. concentrationthe reaction mixture was concentrated to dryness under reduced pressure
  3. washeluted with 40% (V/V) methanol in 0.1% (V/V) aqueous solution of TFA
  4. washFirst, 2-iodo-2'-O-methyladenosine (Compound 47) was eluted
  5. wash2-iodo-3'-O-methyladenosine (Compound 48) was eluted
  6. concentrationBoth fractions were concentrated to dryness

Sources & evidence

ORD record
ord-cf7953d04d664de3b648f811f450011a
Source dataset
uspto-grants-1998_01
Patent number
US05705491

Reaction notes

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