Hydrochloric Acid → 2-Amino-7-(2-cyano-benzyl)-1,7-dihydro-purin-6-one
Reaction equation
O.[C@@H]1([N:11]2[C:21]3[N:20]=[C:18]([NH2:19])[NH:17][C:15](=[O:16])[C:14]=3[N:13]=[CH:12]2)O[C@H](CO)[C@@H](O)[C@H]1O.[C:22]([C:24]1[CH:31]=[CH:30][CH:29]=[CH:28][C:25]=1[CH2:26]Br)#[N:23].Cl>CS(C)=O>[NH2:19][C:18]1[NH:17][C:15](=[O:16])[C:14]2[N:13]([CH2:26][C:25]3[CH:28]=[CH:29][CH:30]=[CH:31][C:24]=3[C:22]#[N:23])[CH:12]=[N:11][C:21]=2[N:20]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Prepared by reacting 20.00 g of guanosine-hydrate with 22.54 g of 2-cyano-benzylbromide in dimethylsulphoxide at 60° C. and subsequent treatment with 57 ml of conc. hydrochloric acid.
Workup
- customPrepared
- customat 60° C.
Sources & evidence
- ORD record
- ord-9626b5ed14ec474db812289f305bbb41
- Source dataset
- uspto-grants-2016_04
- Patent number
- US09321791B2
Reaction notes
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