Diazomethane → HCID 22880806, compound
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
Reactant 3
Product 2
Reagents, catalysts & solvents 1
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
- stirringAfter stirring for one hour at room temperature
- concentrationthe reaction mixture was concentrated to dryness under reduced pressure
- washeluted with 40% (V/V) methanol in 0.1% (V/V) aqueous solution of TFA
- washFirst, 2-iodo-2'-O-methyladenosine (Compound 47) was eluted
- wash2-iodo-3'-O-methyladenosine (Compound 48) was eluted
- 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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