Diisopropylcarbodiimide → Thymidine
Reaction equation
COC1C=CC(C([O:22][CH2:23][C@H:24]2[O:28][C@@H:27]([N:29]3[CH:37]=[C:35]([CH3:36])[C:33](=[O:34])[NH:32][C:30]3=[O:31])[CH2:26][C@@H:25]2[OH:38])(C2C=CC=CC=2)C2C=CC(OC)=CC=2)=CC=1.C(N=C=NC(C)C)(C)C>N1C=CC=CC=1>[C@@H:27]1([N:29]2[CH:37]=[C:35]([CH3:36])[C:33](=[O:34])[NH:32][C:30]2=[O:31])[O:28][C@H:24]([CH2:23][OH:22])[C@@H:25]([OH:38])[CH2:26]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
In a nitrogen-replaced glove box, 5′-O-(4,4′-dimethoxytrityl)thymidine and N,N′-diisoproyl carbodiimide were dissolved in dehydrated pyridine with a concentration of 0.1 mol/L and 0.2 mol/L, respectively.
Sources & evidence
- ORD record
- ord-fb0d3f7858b44c3f81400cbd6481c089
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09410951B2
Reaction notes
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