N-(3-Aminopropyl)morpholine → HCID 18473331, compound

HRID 2227296Notes

Reaction equation

HRID 2227296 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.[NH2:17][CH2:18][CH2:19][CH2:20][N:21]1[CH2:26][CH2:25][O:24][CH2:23][CH2:22]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:17][CH2:18][CH2:19][CH2:20][N:21]2[CH2:26][CH2:25][O:24][CH2:23][CH2:22]2)[N:3]=1

Participants

4

Reactant 2

HCID 61055N-(3-Aminopropyl)morpholineHCID 108011162,6-dichloro-9-cyclopentyl-9H-purine

Product 1

HCID 18473331HCID 18473331, compound

Reagents, catalysts & solvents 1

HCID 8471TriethylamineSolvent

Procedure

2-Chloro-6-[3-(4-morpholinyl)propylamino]-9-cyclopentylpurine is prepared from 2,6-dichloro-9-cyclopentylpurine, 3-aminopropylmorpholine, and triethylamine essentially as described above in Example 1, Scheme A, step b.

Sources & evidence

ORD record
ord-56b16a37e65741289a219104184ada84
Source dataset
uspto-grants-2002_07
Patent number
US06413974B1

Reaction notes

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