4-Chlorophthalic anhydride → HCID 20140094, compound

HRID 1252492Notes

Reaction equation

HRID 1252492 reaction equation
[Cl:1][C:2]1[CH:12]=[C:6]2[C:7]([O:9][C:10](=[O:11])[C:5]2=[CH:4][CH:3]=1)=[O:8].[N:13]1[CH:18]=[CH:17][CH:16]=[C:15]([CH2:19][CH2:20][CH2:21][CH2:22][NH2:23])[CH:14]=1>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:10]([OH:9])=[O:11])=[C:6]([C:7]([NH:23][CH2:22][CH2:21][CH2:20][CH2:19][C:15]2[CH:14]=[N:13][CH:18]=[CH:17][CH:16]=2)=[O:8])[CH:12]=1

Participants

3

Reactant 2

HCID 670444-Chlorophthalic anhydrideHCID 72927Pyridine, 3-(4-aminobutyl)-

Product 1

HCID 20140094HCID 20140094, compound

Procedure

When 5-chlorophthalic anhydride was reacted with 4-(3-pyridinyl)butylamine by the procedure of Example 12, the above compound, mp 152°-154° C. was obtained.

Workup

  1. customthe above compound, mp 152°-154° C. was obtained

Sources & evidence

ORD record
ord-693eeee255c14a38bbcc34d08b2ed4d5
Source dataset
uspto-grants-1988_05
Patent number
US04743610

Reaction notes

Loading…