Pyrrolidine → HCID 21320073, compound
Reaction equation
N1CCCC1.Cl.C[N:8]1[C:16]2[N:11]([CH:12]([CH3:25])[N:13]=[C:14]([NH:17][CH2:18][C:19]3C=CC=[CH:21][CH:20]=3)[CH:15]=2)[CH2:10][CH2:9]1>>[CH3:25][C:12]1[N:11]2[CH2:10][CH2:9][N:8]=[C:16]2[CH:15]=[C:14]([N:17]2[CH2:18][CH2:19][CH2:20][CH2:21]2)[N:13]=1Participants
3
Procedure
Following the above procedure, but substituting N-methyl benzylamine for pyrrolidine, there was prepared N,5-dimethyl-7-benzylamino-2,3-dihydroimidazo[1,2-c]pyrimidine hydrochloride decomposing at 213° C. after recrystallization from ether.
Workup
- customafter recrystallization from ether
Sources & evidence
- ORD record
- ord-d8e1899e8ef84bf881770761331be3bf
- Source dataset
- uspto-grants-1979_05
- Patent number
- US04153695
Reaction notes
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