HCID 53714844, compound → HCID 54526918, compound

HRID 1195443Notes

Reaction equation

HRID 1195443 reaction equation
[F:1][C:2]1[CH:22]=[CH:21][CH:20]=[C:19]([F:23])[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(F)=CC=CC=2F)=C(N(C)C)N=1.C(NC1N=C2C(N=CN2CC2C(F)=CC=CC=2F)=C(N(C)C)N=1)C.FC1C=CC=C(F)C=1CN1C=NC2C1=NC(NC)=NC=2.FC1C=CC=C(F)C=1CN1C=NC2C1=NC(N(C)C)=NC=2.CN(C1N=C2C(N=CN2CC2C(F)=CC=CC=2F)=C(N(C)C)N=1)C.NC1N=C2C(N=CN2CC2C(F)=CC=CC=2F)=C(NC)N=1.CNC1N=C2C(N=CN2CC2C(F)=CC=CC=2F)=C(NC)N=1.NC1N=C2C(N=CN2CC2C(F)=CC=CC=2F)=C(N)N=1.NC1N=C(NC)N=C2C=1N=CN2CC1C(F)=CC=CC=1F.NC1N=C(N(C)C)N=C2C=1N=CN2CC1C(F)=CC=CC=1F.C(NC1N=C2C(N=CN2CC2C(F)=CC=CC=2F)=C(N)N=1)C.[Cl:263]C1N=C2C(N=CN2CC2C(F)=CC=CC=2F)=CN=1>>[Cl:263][C:8]1[N:7]=[C:6]2[C:11]([N:12]=[CH:13][N:5]2[CH2:4][C:3]2[C:2]([F:1])=[CH:22][CH:21]=[CH:20][C:19]=2[F:23])=[C:10]([N:14]([CH3:16])[CH3:15])[N:9]=1

Participants

14

Procedure

9-(2,6-difluorobenzyl)-6-(N,N-dimethylamino)-2-(N-methylamino)-9H-purine; 2-amino-9-(2,6-difluorobenzyl)-6-(N,N-dimethylamino)-9H-purine; 2-(N-ethylamino)-9-(2,6-difluorobenzyl)-6(N,N-dimethylamino)-9H-purine; 9-(2,6-difluorobenzyl)-2-(N-methylamino)-9H-purine; 9-(2,6-difluorobenzyl)-2-(N,N-dimethylamino)-9H-purine; 2,6-bis(N,N-dimethylamino)-9-(2,6-difluorobenzyl)-9H-purine; 2-amino-9-(2,6-difluorobenzyl)-6-(N-methylamino)-9H-purine; 2,6-bis(N-methylamino)-9-(2,6-difluorobenzyl)-9H-purine; 2,6-diamino-9-(2,6-difluorobenzyl)-9H-purine; 6-amino-9-(2,6-difluorobenzyl)-2-(N-methylamino)-9H-purine; 6-amino-9-(2,6-difluorobenzyl)-2-(N,N-dimethylamino)-9H-purine; 2-(N-ethylamino)-6-amino-9-(2,6-difluorobenzyl)-9H-purine and 2-chloro-9-(2,6-difluorobenzyl)-9H-purine.

Sources & evidence

ORD record
ord-44ce459689654706a9f7073e1ff8326e
Source dataset
uspto-grants-1992_05
Patent number
US05110818

Reaction notes

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