3,9-Dichloro-7-methoxyacridine → HCID 71471614, compound

HRID 1506753Notes

Reaction equation

HRID 1506753 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.[N:19]1([CH2:24][CH2:25][CH2:26][CH2:27][NH2:28])[CH2:23][CH2:22][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:19]1[CH2:23][CH2:22][CH2:21][CH2:20]1)=[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 27627624-(Pyrrolidin-1-yl)butan-1-amine

Product 1

HCID 71471614HCID 71471614, compound

Procedure

Following the general procedure of Example 1 and making non-critical variations, but using 6,9-dichloro-2-methoxyacridine and 4-(pyrrolidin-1-yl)butan-1-amine (Step 3), the title compound was obtained; MS (Found M+1=384).

Sources & evidence

ORD record
ord-561b6aba0e4f4a2c9775391ae7e9d23d
Source dataset
uspto-grants-2015_12
Patent number
US09221760B2

Reaction notes

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