Thionyl Chloride → 4-Amino-1-(2-chloroethyl)pyrimidin-2(1H)-one
Reaction equation
O[CH2:2][CH2:3][N:4]1[CH:9]=[CH:8][C:7]([NH2:10])=[N:6][C:5]1=[O:11].S(Cl)([Cl:14])=O>>[Cl:14][CH2:2][CH2:3][N:4]1[CH:9]=[CH:8][C:7]([NH2:10])=[N:6][C:5]1=[O:11]Participants
3
Procedure
B] 1-(2-Chloroethyl)-4-amino-2-1H-pyrimidinone was prepared according to example 14C from 3.8 g 1-(2-hydroxyethyl)-4-amino-2-1H-pyrimidinone and 60 ml thionyl chloride. 3.2 g (97%) of crude product were obtained and used without further purification. Recrystallization was omitted in this case due to decomposition. Rf: 0.51 (ethyl acetate/acetone/acetic acid/H2O 6:2:1:1).
Sources & evidence
- ORD record
- ord-2c363cdce0a7492591780668dec645f1
- Source dataset
- uspto-grants-2004_05
- Patent number
- US06740642B2
Reaction notes
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