(4-Chlorophenyl)(cyclopropyl)methanamine → 2-Chloro-6-[(alpha-cyclopropyl-4-chlorobenzyl)amino]-9-cyclopentylpurine

HRID 1017311Notes

Reaction equation

HRID 1017311 reaction equation
[Cl:1][C:2]1[N:10]=[C:9]2[C:5]([N:6]=[CH:7][N:8]2[CH:11]2[CH2:15][CH2:14][CH2:13][CH2:12]2)=[C:4](Cl)[N:3]=1.[CH:17]1([CH:20]([NH2:28])[C:21]2[CH:26]=[CH:25][C:24]([Cl:27])=[CH:23][CH:22]=2)[CH2:19][CH2:18]1>C(N(CC)CC)C>[Cl:1][C:2]1[N:10]=[C:9]2[C:5]([N:6]=[CH:7][N:8]2[CH:11]2[CH2:15][CH2:14][CH2:13][CH2:12]2)=[C:4]([NH:28][CH:20]([CH:17]2[CH2:18][CH2:19]2)[C:21]2[CH:26]=[CH:25][C:24]([Cl:27])=[CH:23][CH:22]=2)[N:3]=1

Participants

4

Reactant 2

HCID 5155531(4-Chlorophenyl)(cyclopropyl)methanamineHCID 108011162,6-dichloro-9-cyclopentyl-9H-purine

Product 1

HCID 180020772-Chloro-6-[(alpha-cyclopropyl-4-chlorobenzyl)amino]-9-cyclopentylpurine

Reagents, catalysts & solvents 1

HCID 8471TriethylamineSolvent

Procedure

2-Chloro-6-[(α-cyclopropyl-4-chlorobenzyl)amino]-9-cyclopentylpurine is prepared from 2,6-dichloro-9-cyclopentylpurine, α-cyclopropyl-4-chlorobenzylamine, and triethylamine essentially as described above in Example 1, Scheme A, step b.

Sources & evidence

ORD record
ord-4955d126b5c6458d839fd2d9d13b36fb
Source dataset
uspto-grants-2002_11
Patent number
US06479487B1

Reaction notes

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