Dimethyl methylmalonate → HCID 21507539, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[N:5]=[C:4]([N:9]2[CH2:14][CH2:13][O:12][CH2:11][CH2:10]2)[N:3]=1.[CH3:15]C(C(OC)=O)C(OC)=O>>[Cl:8][C:6]1[C:7]([CH3:15])=[C:2]([Cl:1])[N:3]=[C:4]([N:9]2[CH2:14][CH2:13][O:12][CH2:11][CH2:10]2)[N:5]=1Participants
3
Procedure
4,6-Dichloro-5-methyl-2-morpholinopyrimidine was prepared by similar procedure as 4,6-dichloro-2-morpholinopyrimidine (in Method 22) using dimethyl 2-methylmalonate in place of diethyl malonate. LC/MS (m/z): 248.1 (MH+).
Sources & evidence
- ORD record
- ord-ad1e8b4f8ac2474ea31b945ae3f77a02
- Source dataset
- uspto-grants-2013_10
- Patent number
- US08563549B2
Reaction notes
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