1-methyl-1,3,5-triazine-2,4(1h,3h)-dione → 1-Butyl-1,3,5-triazinane-2,4-dione
Reaction equation
[CH2:1]([N:5]1[CH:12]=[N:11][C:9](=[O:10])[NH:8][C:6]1=[O:7])[CH2:2][CH2:3][CH3:4].CN1C=NC(=O)NC1=O>>[CH2:1]([N:5]1[CH2:12][NH:11][C:9](=[O:10])[NH:8][C:6]1=[O:7])[CH2:2][CH2:3][CH3:4]Participants
3
Procedure
Following the procedure described in Preparation 2, Part C, above, but substituting the 1-n-butyl-5-azauracil prepared in Part B, above, for the 1-methyl-5-azauracil, there is prepared 40 gm. (67% yield) of the desired new precursor 5-n-butyl-5,6-dihydro-s-triazine-2,4-(1H,3H)-dione having a melting point of 205° C. to 207° C.
Workup
- customdescribed in Preparation 2, Part C
- customprepared in Part B
Sources & evidence
- ORD record
- ord-3059044b7c484ad3aa2441285e02d297
- Source dataset
- uspto-grants-1983_12
- Patent number
- US04423212
Reaction notes
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