3,9-Dichloro-7-methoxyacridine → HCID 71471684, compound

HRID 1506749Notes

Reaction equation

HRID 1506749 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.[CH3:19][O:20][CH2:21][CH2:22][CH2:23][CH2:24][NH2:25]>>[Cl:1][C:2]1[CH:3]=[C:4]2[C:13](=[CH:14][CH:15]=1)[C:12]([NH:25][CH2:24][CH2:23][CH2:22][CH2:21][O:20][CH3:19])=[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 5339094-Methoxybutan-1-amine

Product 1

HCID 71471684HCID 71471684, compound

Procedure

Following the general procedure of Example 1 and making non-critical variations, but using 6,9-dichloro-2-methoxyacridine and commercially available 4-methoxybutan-1-amine, the title compound was obtained; MS (Found M+1=345).

Sources & evidence

ORD record
ord-a049a660438d45b2988921f5b1bec9dd
Source dataset
uspto-grants-2015_12
Patent number
US09221760B2

Reaction notes

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