3,9-Dichloro-7-methoxyacridine → HCID 71471686, compound

HRID 1506766Notes

Reaction equation

HRID 1506766 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.[CH:19]1([CH2:22][N:23]([CH2:29][CH3:30])[CH2:24][CH2:25][CH2:26][CH2:27][NH2:28])[CH2:21][CH2:20]1>>[Cl:1][C:2]1[CH:3]=[C:4]2[C:13](=[CH:14][CH:15]=1)[C:12]([NH:28][CH2:27][CH2:26][CH2:25][CH2:24][N:23]([CH2:22][CH:19]1[CH2:21][CH2:20]1)[CH2:29][CH3:30])=[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 63957161HCID 63957161, compound

Product 1

HCID 71471686HCID 71471686, compound

Procedure

Following the general procedure of Example 1 and making non-critical variations but using 6,9-dichloro-2-methoxyacridine, N1-(cyclopropylmethyl)-N1-ethylbutane-1,4-diamine (Step 1), the title compound is obtained; MS (Found M+1=412).

Sources & evidence

ORD record
ord-35d93be02b8e40a18bf8089316f923d7
Source dataset
uspto-grants-2015_12
Patent number
US09221760B2

Reaction notes

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