2-Amino-4-chloropyrimidine → HCID 69917682, compound
Reaction equation
[C:1]([O:5][C:6](=[O:34])[NH:7][C@@H:8]([CH2:24][C:25]1[C:33]2[C:28](=[CH:29][CH:30]=[CH:31][CH:32]=2)[NH:27][CH:26]=1)[CH2:9][O:10][C:11]1[CH:12]=[N:13][CH:14]=[C:15]([C:17]2[CH:22]=[CH:21][CH:20]=[C:19]([NH2:23])[CH:18]=2)[CH:16]=1)([CH3:4])([CH3:3])[CH3:2].Cl[C:36]1[CH:41]=[CH:40][N:39]=[C:38]([NH2:42])[N:37]=1>CCO>[C:1]([O:5][C:6](=[O:34])[NH:7][C@@H:8]([CH2:24][C:25]1[C:33]2[C:28](=[CH:29][CH:30]=[CH:31][CH:32]=2)[NH:27][CH:26]=1)[CH2:9][O:10][C:11]1[CH:12]=[N:13][CH:14]=[C:15]([C:17]2[CH:22]=[CH:21][CH:20]=[C:19]([NH:23][C:36]3[CH:41]=[CH:40][N:39]=[C:38]([NH2:42])[N:37]=3)[CH:18]=2)[CH:16]=1)([CH3:4])([CH3:2])[CH3:3]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 80 °C
Procedure
A mixture of Example 121A (0.07 g, 0.153 mmol) and 4-chloro-2-pyrimidinylamine (0.021 g, 0.163 mmol) was dissolved in EtOH (1 mL). The mixture was heated to 80° C. overnight then cooled and evaporated. The product was used without further purification.
Workup
- temperaturethen cooled
- customevaporated
- customThe product was used without further purification
Sources & evidence
- ORD record
- ord-c29fc9ef014f4fab88ef18c21893af61
- Source dataset
- uspto-grants-2004_12
- Patent number
- US06831175B2
Reaction notes
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