9-Chloroacridine → 3-(9-Acridinylamino)-5-hydroxymethylaniline

HRID 1707740Notes

Reaction equation

HRID 1707740 reaction equation
Cl[C:2]1[C:3]2[C:8]([N:9]=[C:10]3[C:15]=1[CH:14]=[CH:13][CH:12]=[CH:11]3)=[CH:7][CH:6]=[CH:5][CH:4]=2.[NH2:16][C:17]1[CH:18]=[C:19]([CH:22]=[C:23]([NH2:25])[CH:24]=1)[CH2:20][OH:21]>>[CH:4]1[C:3]2[C:8](=[N:9][C:10]3[C:15]([C:2]=2[NH:16][C:17]2[CH:24]=[C:23]([CH:22]=[C:19]([CH2:20][OH:21])[CH:18]=2)[NH2:25])=[CH:14][CH:13]=[CH:12][CH:11]=3)[CH:7]=[CH:6][CH:5]=1

Participants

3

Reactant 2

HCID 710139-ChloroacridineHCID 586680(3,5-Diaminophenyl)methanol

Product 1

HCID 3804823-(9-Acridinylamino)-5-hydroxymethylaniline

Procedure

The contacting in step (a) comprises the condensation of 9-chloroacridine and 3,5-diaminobenzyl alcohol to form 3-(9-acridinylamino)-5-hydroxymethylaniline.

Sources & evidence

ORD record
ord-0e61dfd2abf84d28b6f08e760e9ffb4c
Source dataset
uspto-grants-1994_10
Patent number
US05354864

Reaction notes

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