HCID 24904080, compound → HCID 54268312, compound
Reaction equation
[Cl:1][C:2]1[CH:22]=[CH:21][CH:20]=[CH:19][C:3]=1[CH2:4][N:5]1[CH:13]=[N:12][C:11]2[C:6]1=[N:7][C:8](NC)=[N:9][C:10]=2[N:14]([CH3:16])[CH3:15].NC1N=C2C(N=CN2CC2C=CC=CC=2[Cl:40])=C(N(C)C)N=1.C(NC1N=C2C(N=CN2CC2C=CC=CC=2Cl)=C(N(C)C)N=1)C.ClC1C=CC=CC=1CN1C=NC2C1=NC(NC)=NC=2.ClC1C=CC=CC=1CN1C=NC2C1=NC(N(C)C)=NC=2.CN(C1N=C2C(N=CN2CC2C=CC=CC=2Cl)=C(N(C)C)N=1)C.NC1N=C2C(N=CN2CC2C=CC=CC=2Cl)=C(NC)N=1.ClC1C=CC=CC=1CN1C=NC2C1=NC(N(C)C)=NC=2NC.NC1N=C2C(N=CN2CC2C=CC=CC=2Cl)=C(N)N=1.NC1N=C(NC)N=C2C=1N=CN2CC1C=CC=CC=1Cl.NC1N=C(N(C)C)N=C2C=1N=CN2CC1C=CC=CC=1Cl.C(NC1N=C2C(N=CN2CC2C=CC=CC=2Cl)=C(N)N=1)C.ClC1N=C2C(N=CN2CC2C=CC=CC=2Cl)=CN=1>>[Cl:40][C:8]1[N:7]=[C:6]2[C:11]([N:12]=[CH:13][N:5]2[CH2:4][C:3]2[CH:19]=[CH:20][CH:21]=[CH:22][C:2]=2[Cl:1])=[C:10]([N:14]([CH3:16])[CH3:15])[N:9]=1Participants
14
Reactant 13
Product 1
Procedure
9-(2-chlorobenzyl)-6-(N,N-dimethylamino)-2-(N-methylamino)-9H-purine; 2-amino-9-(2-chlorobenzyl)-6-(N,N-dimethylamino)-9H-purine; 2-(N-ethylamino)-9-(2-chlorobenzyl)-6-(N,N-dimethylamino)-9H-purine; 9-(2-chlorobenzyl)-2-(N-methylamino)-9H-purine; 9-(2-chlorobenzyl)-2-(N,N-dimethylamino)-9H-purine; 2,6-bis(N,N-dimethylamino)-9-(2-chlorobenzyl)-9H-purine; 2-amino-9-(2-chlorobenzyl)-6-(N-methylamino)-9H-purine; 9-(2-chlorobenzyl)-2-(N,N-dimethylamino)-6-(N-methylamino)-9H-purine; 2,6-diamino-9-(2-chlorobenzyl)-9H-purine; 6-amino-9-(2-chlorobenzyl)-2-(N-methylamino)-9H-purine; 6-amino-9-(2-chlorobenzyl)-2-(N,N-dimethylamino)-9H-purine; 2-(N-ethylamino)-6-amino-9-(2-chlorobenzyl)-9H-purine and 2-chloro-9-(2-chlorobenzyl)-9H-purine.
Sources & evidence
- ORD record
- ord-75f59c6914074d0a91e06f0c8e24eea5
- Source dataset
- uspto-grants-1992_05
- Patent number
- US05110818
Reaction notes
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