Ethanol → 2-Benzyloxymethyl-4(3H)-pteridinone
Reaction equation
N[C:2]1[C:11]2[C:6](=[N:7][CH:8]=[CH:9][N:10]=2)[N:5]=[C:4]([CH2:12][O:13][CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[N:3]=1.C([OH:23])C>[OH-].[Na+]>[CH2:14]([O:13][CH2:12][C:4]1[NH:3][C:2](=[O:23])[C:11]2[C:6](=[N:7][CH:8]=[CH:9][N:10]=2)[N:5]=1)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Obtained using the procedure described in section b of Example 9, starting with 10.0 g (0.037 mole) of crude 4-amino-2-(benzyloxymethyl)pteridine in 300 ml of 5% aqueous sodium hydroxide. Heating time: 2 hours at 80° C. Yld: 8.2 g (83%), m.p. 157°-159° C. (ethanol).
Workup
- customObtained
- temperatureHeating time
- custom2 hours
- customat 80° C
Sources & evidence
- ORD record
- ord-61a7494901f54b37947756cbcfb90b9f
- Source dataset
- uspto-grants-1993_12
- Patent number
- US05270465
Reaction notes
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