4-Chlorophthalic anhydride → HCID 69156451, compound

HRID 750119Notes

Reaction equation

HRID 750119 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[O:10])[O:8][C:6](=O)[C:5]2=[CH:11][CH:12]=1.Cl.[CH3:14][O:15][C:16](=[O:25])[C:17]1[CH:22]=[CH:21][C:20]([CH2:23][NH2:24])=[CH:19][CH:18]=1>>[CH3:6][O:8][C:9]([C:4]1[N:24]([CH2:23][C:20]2[CH:21]=[CH:22][C:17]([C:16]([O:15][CH3:14])=[O:25])=[CH:18][CH:19]=2)[C:6](=[O:8])[C:5]2[C:4]([C:9]=1[OH:10])=[CH:3][C:2]([Cl:1])=[CH:12][CH:11]=2)=[O:10]

Participants

3

Reactant 2

HCID 670444-Chlorophthalic anhydrideHCID 2729253Methyl 4-(aminomethyl)benzoate hydrochloride

Product 1

HCID 69156451HCID 69156451, compound

Procedure

The present compound was synthesized according to the method shown in Reference Example 8 and using 4-chloro phthalic anhydride and 4-(aminomethyl)benzoic acid methyl ester hydrochloride.

Workup

  1. customThe present compound was synthesized

Sources & evidence

ORD record
ord-343f958d04b7400caf0da8c983683d7a
Source dataset
uspto-grants-2008_07
Patent number
US07402595B2

Reaction notes

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