Hydrochloric Acid → HCID 178479374, compound

Reaction equation

[NH2:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5]([OH:7])=[O:6].[NH2:11][C:12]([NH2:14])=[NH:13].[ClH:15]>>[NH:1]([C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5]([OH:7])=[O:6])[C:12]([NH2:13])=[NH:11].[ClH:15].[NH:13]([C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5]([OH:7])=[O:6])[C:12]([NH2:14])=[NH:11]

Participants

Reactant 3

HCID 313Hydrochloric Acid

HCID 3520Guanidine

HCID 74193-Aminobenzoic Acid

Product 2

HCID 178479374HCID 178479374, compound

HCID 178512495HCID 178512495, compound

Procedure

3-guanidinobenzoic acid was prepared from 3-aminobenzoic acid by the method of Miller, et al., cited in Example 1C. The guanidine was treated with ethereal hydrogen chloride to give 3-guanidino-benzoic acid hydrochloride.

Sources & evidence

ORD record: ord-a0fe656b278c44d69e3ab92ac531b551
Source dataset: uspto-grants-1992_02
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05086069

Reaction notes

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