Methylamine → 7-chloro-N-methyl-6-phenylimidazo[1,2-a]pyrimidin-5-amine
Reaction equation
Cl[C:2]1[N:7]2[CH:8]=[CH:9][N:10]=[C:6]2[N:5]=[C:4]([Cl:11])[C:3]=1[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.[CH3:18][NH2:19]>CO>[Cl:11][C:4]1[C:3]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[C:2]([NH:19][CH3:18])[N:7]2[CH:8]=[CH:9][N:10]=[C:6]2[N:5]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
850 mg 5,7-dichloro-6-phenylimidazo[1,2-a]pyrimidine (prepared as described for example 1) was dissolved in 18 mL of a 8M Solution of MeNH2 in methanol and stirred at room temperature for 1.5 h. The product precipitated upon dilution with water and cooling to 0° C. The solid material was collected by filtration and washed twice with water to yield the desired material.
Workup
- customThe product precipitated upon dilution with water
- temperaturecooling to 0° C
- filtrationThe solid material was collected by filtration
- washwashed twice with water
Sources & evidence
- ORD record
- ord-09b2a4f22d514437803867b5f642cbca
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08957064B2
Reaction notes
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