3,9-Dichloro-7-methoxyacridine → HCID 71471616, compound

HRID 1506757Notes

Reaction equation

HRID 1506757 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]2[C:13](=[CH:14][CH:15]=1)[C:12](Cl)=[C:11]1[C:6]([CH:7]=[CH:8][C:9]([O:17][CH3:18])=[CH:10]1)=[N:5]2.[NH2:19][CH2:20][CH2:21][CH2:22][CH2:23][N:24]([CH2:29][CH3:30])[S:25]([CH3:28])(=[O:27])=[O:26]>>[Cl:1][C:2]1[CH:3]=[C:4]2[C:13](=[CH:14][CH:15]=1)[C:12]([NH:19][CH2:20][CH2:21][CH2:22][CH2:23][N:24]([CH2:29][CH3:30])[S:25]([CH3:28])(=[O:27])=[O:26])=[C:11]1[C:6]([CH:7]=[CH:8][C:9]([O:17][CH3:18])=[CH:10]1)=[N:5]2

Participants

3

Reactant 2

HCID 665773,9-Dichloro-7-methoxyacridineHCID 86720059HCID 86720059, compound

Product 1

HCID 71471616HCID 71471616, compound

Procedure

Following the general procedure of Example 1 and making non-critical variations, but using 6,9-dichloro-2-methoxyacridine and N-(4-aminobutyl)-N-ethylmethanesulfonamide (Step 3), the title compound was obtained; MS (Found M+1=436).

Sources & evidence

ORD record
ord-53b32c4a6c6d4742b882bbf173c0ab6c
Source dataset
uspto-grants-2015_12
Patent number
US09221760B2

Reaction notes

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