Ammonia → HCID 20393842, compound
Reaction equation
N.[NH2:2][CH:3]1[CH2:8][N:7]([CH3:9])[CH2:6][CH2:5][N:4]1[C:10]1[N:15]=[CH:14][C:13]([S:16][CH3:17])=[C:12]([Cl:18])[N:11]=1>C(O)C>[ClH:18].[NH2:2][CH:3]1[CH2:8][N:7]([CH3:9])[CH2:6][CH2:5][N:4]1[C:10]1[N:15]=[CH:14][C:13]([S:16][CH3:17])=[C:12]([Cl:18])[N:11]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
In the same way as in Example 1, but replacing the ethylamine by ammonia, 2-amino-4-N-methylpiperazino-6-chloro-5-methylthio-pyrimidine is prepared. M.p. 191°-192° C. (ethanol).
Workup
- customis prepared
Sources & evidence
- ORD record
- ord-92d9f53da5f24988b1a08c5af07c0955
- Source dataset
- uspto-grants-1979_09
- Patent number
- US04166852
Reaction notes
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