3,9-Dichloro-7-methoxyacridine → HCID 71471619, compound

HRID 1506760Notes

Reaction equation

HRID 1506760 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]([CH2:28][CH3:29])[C:25](=[O:27])[CH3:26]>>[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]([CH2:28][CH3:29])[C:25](=[O:27])[CH3:26])=[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 83969222HCID 83969222, compound

Product 1

HCID 71471619HCID 71471619, 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-ethylacetamide (Step 1), the title compound was obtained; MS (Found M+1=400).

Sources & evidence

ORD record
ord-cb269985b58c4c5ba6a98df82c1d092d
Source dataset
uspto-grants-2015_12
Patent number
US09221760B2

Reaction notes

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